Antimicrobial Secondary Metabolites from the Mangrove Plants of Asia and the Pacific

Abstract

Microbes such as the White Spot Syndrome Virus account for severe losses in the shrimp farming industry globally. This review examines the literature on the mangrove plants of Asia and the Pacific with antibacterial, antifungal, or antiviral activities. All of the available data published on this subject were collected from Google Scholar, PubMed, Science Direct, Web of Science, ChemSpider, PubChem, and a library search from 1968 to 2022. Out of about 286 plant species, 119 exhibited antimicrobial effects, and a total of 114 antimicrobial natural products have been identified including 12 with MIC values below 1 µg/mL. Most of these plants are medicinal. The mangrove plants of Asia and the Pacific yield secondary metabolites with the potential to mitigate infectious diseases in shrimp aquaculture.

1. Introduction

The global shrimp and prawn aquaculture industry is regularly threatened by outbreaks of microbial infections [1] that require antibiotics, antifungals, and antiviral agents participating in the selection of multidrug-resistant strains of microbes, pausing the grim scenario of the emergence of a “superbug” that could wipe out the global supply of penaeids [2]. In this context, there is an urgent necessity to search for antimicrobial agents with original chemical frameworks, and such molecules could come from the flora of Asia and the Pacific, which is the oldest, largest, and richest on Earth, especially seashores, tidal rivers, and mangrove plants.

Mangroves are ecosystems of the tropical and subtropical seashores, estuaries, and tidal rivers characterized by a halophytic flora of mainly trees and shrubs divided into true mangrove or mangrove-associated species. True mangrove species are restricted to mangroves whereas mangrove-associated species are found along the seashores, and even inland. There are estimates of about 54 true mangrove plant species and 60 mangrove-associated species globally, which are home to shrimps, prawns, crabs, and fish [3]. Most mangrove species grow in Asia and the Pacific [4]. Examples of true mangrove plant species are Excoecaria agallocha L. (land zone), Bruguiera gymnorhiza (L.) Savigny, Rhizophora stylosa Griff. (intermediate zone), Avicennia alba Bl, and Aegiceras corniculatum (L.) Blanco (fringing zone) [5]. Even though most of the global fish catches are directly or indirectly dependent on mangroves, these are on their way to extinction due to logging, agriculture, aquaculture, and urbanization, with an estimate of about 2–8% loss of surface per year [6]. Shrimps, prawns, and fish farming are the greatest threat to mangroves with, for example, approximately half of the 279,000 ha of mangroves in the Philippines lost from 1951 to 1988 [7]. Another aggravating factor is global warming, and consequently, a rise in sea levels that interfere with the growth of true mangrove plants.

Most plants in mangroves are Angiosperms organized phylogenetically into 11 major taxa or clades organized in three groups: (i) Basal Angiosperms: Protomagnoliids, Magnoliids, Monocots, Eudicots; (ii) Core Angiosperms: Core Eudicots, Rosids, Fabids, Malvids; and (iii) Upper Angiosperms: Asterids, Lamiids, and Campanulids. Within each clade, plants yield specific secondary metabolites to control and even communicate with phytopathogenic bacteria and fungi. Plants are challenged by phytopathogenic bacteria, fungi, and viruses and produce a vast array of antimicrobial secondary metabolites [8]. These antimicrobial principles fall into two main categories: phytoanticipins and phytoalexins. Phytoanticipins are antimicrobials present in plant tissues before pathogen challenges or inactive immediate precursors of phytoalexins [8].

Phytoanticipins and phytoalexins are mainly either phenolics, terpenes, or alkaloids with various levels of solubility in water and are extractable with water, polar organic (methanol, ethanol), mid-polar solvents (chloroform, dichloromethane, ethyl acetate), and non-polar solvents (hexane, petroleum ether) [9]. The measurement of the antibacterial and antifungal strength of extracts and secondary metabolites in vitro is quantitatively based on the minimum inhibiting concentration (MIC) and several thresholds of activity have been proposed [10]. Qualitatively, antibacterial and antifungal strength are appreciated by halos developed around a paper disc or an agar well expressed in the inhibition zone diameter (IZD) [10].

Colette et al. (2022) noted that the presence of Atriplex jubata S. Moore evoked some levels of remediation in the shrimp farms of New Caledonia [11] and this review aims to attempt to answer the following points: What is the current knowledge on the distribution of antibacterial, antifungal, and antiviral principles from the mangrove plants of Asia and the Pacific? What are the strongest antimicrobial principles isolated thus far from these plants? What is the spectrum of activity of the antimicrobial principles? What are the medicinal values of these plants? What is the potential usefulness of these plants as remediation of shrimp farming? We hypothesize that a shrimp or prawn farming system preserving healthy mangroves could be a mean to solve the increasing problem of infection.

2. Distribution of Antibacterial, Antifungal, and Antiviral Principles Various Mangrove Plants

The enumeration of mangrove and mangrove-associated plants is provided in Table S1, and the chemical structures of the antimicrobial secondary metabolites identified from these plants is given Figure S1.

2.1. Subclass Lycopodidae

The only lycopod associated with mangroves is Lycopodium carinatum Desv. ex Poir., for which no antimicrobial activities have been recorded thus far.

2.2. Subclass Polypodiidae

Aqueous and polar organic extracts of ferns of the mangrove are moderately broad-spectrum antibacterial and antifungal (Table 1). Data on the antiviral properties of ferns are lacking. The methanol extract of Stenochlaena palustris (Burm. f.) Bedd. (25 µL/6 mm disc of a 100 mg/mL solution) evoked halos against Staphylococcus aureus, Bacillus subtilis, Escherichia coli, Klebsiella pneumoniae, Salmonella typhi, Penicillium chrysogenum, Aspergillus niger, and Saccharomyces cerevisae [12]. From the leaves of this fern was identified the flavonol glycoside stenopalustroside A (1), which strongly repressed the Staphylococcus epidermidis [13]. Antimicrobials in this subclass are mainly phenolics. Other ferns with broad-spectrum antibacterial and antifungal properties are Nephrolepis biserrate (Sw.) Schott, Drynaria quercifolia (L.) J. Sm., Drymoglossum piloselloides (L.) Presl., Pyrrosia piloselloides (L.) Farw., Microsorum punctatum (L.) Copel. [14,15,16], Phymatosorus scolopendria (Burm. f.) Pic. Serm. [17], Platycerium coronarium (O.F. Müll.) Desv. [18], and the true mangrove fern Acrostichum aureum L. [19,20,21]. Of note, the ethyl acetate extract of roots of Acrostichum speciosum L., which is a true mangrove fern, was bactericidal for E. coli with the MIC/MBC of 40/40 µg/mL [21].

2.3. Subclass Cycadaceae

The ethyl acetate extract of Cycas rumphii Miq. developed halos against Staphylococcus albus whereas the methanol extract (20 mg/mL solution per disc) hampered the growth of S. aureus and E. coli [22]. Later, the methanol extract of leaves (paper disc impregnated with 20 mg/mL solution) repressed S. aureus (ATCC 25953) [22]. Note that the Cycadaceae have not been much studied for their antimicrobial effects (Table 1) [23].

2.4. Subclass Magnoliidae

Mangrove plants in this subclass produce most of, and a broad spectrum of antimicrobial secondary metabolites.

2.4.1. Clade Protomagnoliids

Plants in the clade are not found in mangroves.

2.4.2. Clade Magnoliids

Plants in this clade are not common in mangroves and principally yield antimicrobial isoquinoline alkaloids and lignans (Table S2). In the Lauraceae, the filamentous climber Cassytha filiformis L. yields the aporphine dicentrine (2), which inhibits the growth of Cladosporium clodosporioides (Table S2) [24]. Hernandia nymphaeifolia (C. presl.) Kubitzki (Hernandiaceae) produces the dibenzyl butyrolactone lignan deoxypodophyllotoxin (3), which is strongly active against HSV (Table S2) [25]. In the family Annonaceae, the hexane extract of stem bark of Annona glabra L. exhibited antibacterial and antifungal properties on account of kaurane diterpenes (Table S2) [26].

2.4.3. Clade Monocots

Plants in this clade are mainly mangrove-associated with organic extracts being moderately broad-spectrum antibacterial and antifungal and producing mainly antimicrobial phenolics (Table 2). For instance, the ethanol extract of rhizomes of Lasia spinosa (L.) Thwaites developed halos with S. aureus, S. epidermidis, S. pyogenes, S. dysenteriae, E. coli, V. cholerae, E. aerogenes, P. aeruginosa, C. albicans, A. niger, and S. cerevisae (500 µg/disc) [27,28]. Other instances are Phoenix paludosa Roxb. [29,30], Saribus rotundifolius (Lam.) Bl. [31], Cyperus scariosus R. Br. [32], Eleocharis dulcis (Burm. f.) Trin. ex Hensch. [33,34], Pandanus tectorius Parkinson [35], the true mangrove Nypa fruticans Wurm. [35], Areca catechu L. [31], Phragmites vallatoria Veldkamp [36], Ruppia maritima L. [37], and Flagellaria indica L. [38]. The ethanol extract of Flagellaria indica L. at the concentration of 12.5 µg/mL repressed DV by 45.5% [39,40]. In the family Orchidaceae, an aqueous extract of Aerides odoratum Reinw. ex Bl. repressed the E. coli [41] and the chloroform extract of pseudobulbs of Cymbidium finlaysonianum Wall. ex Lindl. moderately retrained T. Mentagrophytes (MIC: 250 µg/mL) [42]. From this orchid, the phytoalexin stilbene batatasin III (4) was active against Gram-positive bacteria [43] as well as phytopathogenic filamentous fungi [44]. Gigantol (5) and batatasin III exhibited meek activity with HSV-1 and -2 [45]. The phenanthrene moscatin (6) from Dendrobium moschatum (Buch. -Ham.) Sw. is a moderate antibacterial [46]. Other examples of antibacterial and antifungal phenolics from the Monocots are meridinol (7) [47], tricin (8) [48,49], and naringenin (9) [50,51] (Table 2).

2.4.4. Clade Core Eudicots

Plants in this clade are not found in mangroves.

2.4.5. Clade Core Eudicots

Plants in this clade are not found in mangroves.

2.4.6. Clade Rosids

The ethanol extract of the leaves of Cayratia trifolia (L.) Domin (Vitaceae) inhibited the growth of S. aureus [52]. This climber produces antibacterial and antifungal as well as antivirals as in ɛ -viniferin (12) piceid (13), and resveratrol (14) (Table S2), [53,54,55,56,57,58,59].

2.4.7. Clade Fabids

Fabids principally yield antimicrobial phenolics (Table S2).

Order Malpighiales: Organic polar, mid-polar, and non-polar extracts of Calophyllum inophyllum L. (Clusiaceae) are broadly antimicrobial [60,61,62]. Of note, the methanol extract of latex very strongly hindered S. aureus with an IC₅₀ of 1.1 µg/mL and Trichophyton rubrum with an IC₅₀ of 3.3 µg/mL [63]. The hexane extract of seeds strongly restrained HIV-1 at the concentration of 10 µg/mL [64]. Inophyllum B (15), inophyllum B acetate (16), and inophyllum P (17) from the leaves blocked HIV reverse transcriptase respectively, while inophyllum B (15) and P (17) inhibited HIV with IC₅₀ values of 1.4 and 1.6 µM, respectively (Table S2) [61].

In the Euphorbiaceae, extracts of leaves of Excoecaria agallocha L. moderately repressed a broad array of bacteria and yeasts [64,65,66,67]. The ethanol extract of leaves inhibited the replication of the ECMV (EC₅₀:16.7 µg/mL), HIV (EC₅₀: 7.3 µg/mL), NDV, and SFV [68]. This vesicant tree yields 12-deoxyphorbol 13-(3E,5E-decadienoate) (18) with very strong antiretroviral effects (Table S2) [69]. Suregada glomerulata (Bl.) Baill. yields the alkaloid 5β-carboxymethyl-3α-hydroxy-2β-hydroxymethyl-1- methylpyrrolidine (19), which curbed HIV-1 replication (Table S2) [70].

Plants in the Rhizophoraceae are tanniferous and have antibacterial activities as in Bruguiera cylindrica (L.) Bl. [71], Bruguiera gymnorhiza (L.) Savigny [72], Bruguiera sexangula (Lour.) Poir., Ceriops decandra Griff.) Ding Hou [28,63], Ceriops tagal (Perr.) C.B. Rob. [71], Kandelia candel (L.) Druce [73,74], Rhizophora apiculata Bl. [75], and Rhizophora stylosa Griff. [71,76]. The hydrolysable tannin fraction of the bark of the latter weakly inhibited the growth of A. calcoaceticus, B. lichenifornis, P. mirabilis, and S. saprophyticus [77]. Other antibacterials in this family are 2,6-dimethoxy-p-benzoquinone (20) as well as gallic acid (21) [78,79] (Table S2), [78,79,80,81,82,83,84,85,86,87,88,89,90,91,92,93].

16-Hydroxypimar-8(14)-en-15-one (22) from the roots of Ceriops tagal (Perr.) C.B. Rob. Moderately restrained a broad-spectrum of bacteria (Table S2) [80]. Diterpenes are often liposoluble, explaining perhaps the suppression of a broad-spectrum of bacteria and fungi including B. pumilus with a MIC value of 15.6 µg/mL by the benzene extract of the wood of C. decandra [94]. The presence of tannins and phenolics most probably account for the antiviral effects observed in B. cylindrica, Rhizophora mucronata Lam., R. apiculata, B. gymnorhiza [72], C. decandra [68]. Other examples of water soluble antibacterials are the cyclohexylideneacetonitrile derivatives from B. gymnorhiza, which strongly repressed HBV [69].

Order Fabales: Aqueous, polar and mid-polar extracts of Fabaceae are moderately broad-spectrum antibacterial and antifungal, as observed with Caesalpinia bonduc (L.) Roxb [95] (Table S2) [96]. The methanol extract of the seed coat of this climber strongly restrained P. aeruginosa, S. aureus, and B. cereus (MIC: 22 µg/mL) [97]. This extract given to Wistar rats subcutaneously at a dose of 25 mg/kg body weight once a day for 10 days evoked a reduction in lung abscesses induced by P. aeruginosa [97]. The active principle here are diterpenes including bondenolide (23) [96] and neocaesalpin P (24) [98].Other examples of Fabaceae yielding antibacterial or antifungal organic polar or mid-polar extracts are- Canavalia maritima Thouars [99], the true mangrove tree Cynometra iripa Kostel. [100], Cynometra ramiflora Miq. [101], Derris scandens (Aubl.) Pittier [17], Derris trifoliata Lour. [102], Inocarpus fagifer (Parkinson) Fosb. [17], Sindora siamensis Teysm. ex Miq. [103], Pongamia pinnata (L.) Pierre [104], and Cathormion umbellatum (Vahl) Kosterm. [105]. Plants in this family yield antibacterial and/or antifungal isoflavonoids such as lupalbigenin (25) and derrisisoflavone A (26) from Derris scandens (Aubl.) Pittier [106,107,108,109] (Table S2) [107,109,110]. Other examples are santal (27), scandenin A (28) dalpanitin (29), vicenin 3 (30), derrisisoflavone C (31), and 5,7,4′-trihydroxy-6,8-diprenylisoflavone (32) [107]. Organic and aqueous extracts in this family are often antiviral, as in D. scandens with HSV-1 (IC₅₀: 60 μg/mL) PV and MV as well as Cynometra ramiflora Miq. with DV-2 [111], and Derris trifoliata Lour. with HIV [112,113]. As for antiviral principles, isoflavone deguelin (33) was active against HCMV [113,114] whereas rotenone (34) restrained HSV-1 and -2. D. trifoliata yields the strong antibacterial and anticandidal lupinifolin (35) (Table S2) [115,116,117]

Order Fagales: Organic polar and mid-polar extract of fruits and leaves of the tanniferous Casuarina equisetifolia L. (Casuarinaceae) are broadly antibacterial and antifungal [118,119,120].

Order Rosales: In the Moraceae, the methanol extract of the bark of Ficus microcarpa L.f. (40 µL of a 10 mg/mL solution on 6 mm disc) developed halos with B. brevis, B. cereus, B. subtilis, E. coli, and A. polymorph [121]. From this tree, the flavanols (+) (2R,3S) afzelechin (36) and (-)(2R,3R) epiafzelechin (37) weakly repressed HSV-1 (Table S2) [122].

2.4.8. Clade Malvids

Antimicrobials in this vast Clade are diverse (Table S2).

Order Myrtales: Polar and mid-polar organic extracts of Combretum quadrangulare Kurz (Combretaceae) [123] and Terminalia catappa L. (Combretaceae) are antibacterial and anticandidal [124,125] probably due to ellagitannins such as corilagin (38) [81,126] (Table S2) [127,128] and other phenolics. Phenolic fraction from the fruits of T. catappa strongly repressed S. aureus, B. subtilis, E. faecalis, and L. monocytogenes with the MIC values of 15.6, 15.6, 7.8, and 15.6 µg/mL, respectively [129]. Other antimicrobials in this family are triterpenes, probably explaining the strong activity of the hexane extract of Lumnitzera racemosa Willd. with B. cereus and E. coli [21]. The ethanol extract of barks of this shrub repressed NVD, VV, EMCV, and SFV [130]. Aqueous extracts from Combretaceae plants are often antiviral, as in the pericarps of T. catappa with HSV-2 [131] or C. quadrangulare blocking HIV integrase with the IC₅₀ of 2.9 µg/mL [132].

The methanol extract of the true mangrove shrub Pemphis acidula J.R. & G. Forst (Lythraceae) hindered a broad-spectrum of bacteria [133,134]. Essential oils of Melaleuca cajuputi Roxb. and Melaleuca quinquenervia (Cav.) S.T. Blake (Myrtaceae) are strongly and broadly antibacterial and antifungal [135,136,137,138]. The essential oil of M. quinquenervia repressed Phytophthora cactorum [139] and was strongly fungicidal for filamentous fungi [140].

In the family Sonneratiaceae, polar and mid-polar organic and aqueous extracts of the true mangrove trees Sonneratia apetala Buch-Ham., Sonneratia griffithii Kurtz., and Sonneratia ovata Back. are bacterial and antifungal [21,141,142,143,144,145]. S. griffithii yields strongly antibacterial lupane triterpenes such as 3β-hydroxy-lup-9(11),12-diene, 28-oic acid (39), lupeol (40), and lupan-3β-ol (41) (Table S2) [146]. Antiviral triterpenes are present in Sonneratiaceae plants [147].

Order Brassicales: Polar organic extracts of Azima sarmentosa (Bl.) B. & H and Azima tetracantha Lam. (Salvadoraceae) inhibited the growth of bacteria and fungi [148,149].

Order Malvales: In the family Malvaceae, organic polar extracts of Hibiscus tiliaceus L. and Thespesia populnea (L.) Soland. ex Correa restrained a broad array of bacteria [150,151]. T. populnea yields the cadalane sesquiterpenes populene C (42) and D (43), mansonone D (44) and E (45), 7-hydroxycadalene (46), gossypol (47), and (+) 6,6’-methoxygossypol (48) with strong activity toward Gram-positive bacteria (Table S2) [152]. The ethanol extract of flowers of T. populnea strongly hindered VSV, CV B4, and RSV (EC₅₀: 20 μg/mL) [153] whereas the methanol extract of Malachra capitata (L.) L. was active against the FMDV [154]. The petroleum ether extract of the leaves of Kleinhovia hospita L. strongly retrained E. coli and A. jejunii with the MIC values of 35.7 and 38 µg/mL, respectively [155,156], while the ethanol extract of the bark yielded a MIC value of 4 µg/mL with S. aureus [17]. From this plant, the steroids (9R,10R, 23R)-21,23:23,27-diepoxycycloarta-1,24-diene-3,27-dione (49) and (9R,10R,21S,23R)-21/23,23/27-diepoxy-21-methoxycycloartan-1,24-diene-3,27-dione (50) are strongly active (Table S2) [156].

Sterculiaceae plants are often antimicrobial as in the dichloromethane extract Heritiera littoralis Aiton with M. madagascariense and M. indicus [157,158]. From this tree, the flavonol glycoside afzelin (51) is strongly antibacterial and antiviral (Table S2) [55,159,160,161,162,163].

Other antimicrobial principles in this true mangrove tree are taraxerol (52), friedelin (53), and astilbin (54) [164]. The ethanol extract of the bark of Heritiera fomes Buch. Ham. developed halos with S. epidermidis, S. pyogenes, E. coli, E. aerogenes, Pseudomonas sp. [28], and K. rhizophilia [164].

Order Sapindales: Organic polar extracts of the true mangrove trees Aglaia cucullata Pellegr., Xylocarpus granatum J. Koenig, and Xylocarpus moluccensis (Lam.) M. Roem (Meliaceae) displayed antibacterial properties [28,165,166] (Table S2) [144–146,148). Phytoalexins in this family are limonoids such as in the antiretroviral sundarbanxylogranin B (55) from the seeds of X. granatum [167] or thaixylomolin I (56) and K (57) isolated from the seeds of X. moluccensis [168]. Another example is krishnolide A (58) [169]. From the latter, moluccensin I from the fruits moderately inhibited the growth of S. hominis and E. faecalis [170]. The limonoid catabolite dihydrofuranone 3-(1-hydroxyethyl)-2,2-dimethyl-4-butyrolactone (59) from the leaves of X. granatum is a strong repressor of the phytopathogenic fungi Blumeria graminis [171].

In the Rutaceae, essential oils of Acronychia pedunculata (L.) Miq. and Limnocitrus littoralis (Miq.) Swingle are antibacterial and antifungal [172,173,174]. The ethanol extract of the former was active toward C. albicans, A. niger, and C. neoformans [175]. The acridone pharmacophore [176] intercalates into microbial DNA [177] and represses WSSV [178]. A. pedunculata yields very strong antistaphylococcal acridone alkaloids [179] as well as the prenylated acetophloroglucinol acrovestone (60) [177] (Table S2) [180].

Antimicrobials in the family Sapindaceae are mainly triterpene saponins and triterpenes the later soluble lipid. The petroleum ether of Allophylus cobbe (L.) Raeusch strongly inhibited the growth of Shigella sonnei, Salmonella paratyphi, and C. neoformans with the MIC values of 31.2 µg/mL [178,179,180,181]. The methanol extract of the leaves of Harpullia arborea (Blanco) Radlk repressed a broad-spectrum of bacteria and fungi [182] whereas the ethanol extract of leaves was active against HCV [183] on probable account of simple phenolic glycosides [184].

The methanol extract of leaves of Quassia indica (Gaertn.) Nooteboom (Simaroubaceae) developed halos with E. coli, S. aureus, A. Niger, and C. albicans [185].

Order Santalales: Plants in the Loranthaceae generate antimicrobial phenolics such as the flavonol glycoside quercitrin isolated from the leaves of Dendrophthoe pentandra (L.) Miq. (100 µg/mL/6 mm disc) [186]. These are soluble in methanol explaining the antibacterial properties of Macrosolen cochinchinensis (Lour.) Tiegh [187] or Viscum orientale Willd. [188]. The organic polar extracts of Olax scandens Roxb. and Ximenia americana L. (Olacaceae) are antibacterial and antifungal [189,190,191]. Phytoalexins here are often polyacetylene fatty acids extractable with non-polar solvent from which the halos developed against B. subtilis, Enterococcus faecalis, P. aeruginosa, and K. pneumoniae with the hexane extract of the leaves of Olax scandens Roxb. [192]. The methanol extract of the stembark of X. americana strongly inhibited the replication of HIV [193].

Order Caryophyllales: In the order Caryophyllales, a fatty acid fraction of Sesuvium portulacastrum (L.) L. (Aizoaceae) as well as the essential oil moderately hindered a broad-spectrum of bacteria and fungi [194,195]. The ethanol extract of leaves was active against HBV [130]. The polar organic extract of Salicornia brachiata Miq. and Suaeda maritima (L.) Dumort. (Chenopodiaceae) displayed broad-spectrum antibacterial, antifungal, and antiviral properties [196,197]. The fatty acid fraction of the aerial parts of S. brachiata Miq. moderately restrained B. subtilis S. aureus and methicillin-resistant S. aureus [198]. The ethanol extract of the leaves of S. maritima was active against the EMCV [130]. The organic polar extract of the true mangrove tree Aegialitis rotundifolia Roxb. and Limonium tetragonium Bullock (Plumbaginaceae) are antibacterial and antifungal [199,200]. The methanol extract of the roots of L. tetragonium Bullock blocked HIV-1 reverse transcriptase [201].

2.4.9. Clade Asterids

Plants in this clade yield antimicrobial triterpenes (Table S2).

In the order Ericales, the ethanol extract of the bark of the true mangrove tree Diospyros littorea (R. Br.) Kosterm. (Ebenaceae) developed halos with Streptococcus sp., S. aureus, Aeromonas hydrophila, and Vibrio parahaemolyticus [62].

Antimicrobial principles in the Lecythidaceae are mainly triterpene saponins that are soluble in polar organic and aqueous extracts, explaining why plants in the genus Barringtonia J.R. Forst. & G. Forst. are antibacterial and antifungal. The methanol extract of leaves of Barringtonia acutangula (L.) Gaertn. hindered C. albicans and Candida tropicalis with the MIC values of 31.2 and 62.5 µg/mL, respectively [202,203]. Other examples include the methanol extract of Barringtonia asiatica (L.) Kurz [204] or Barringtonia racemosa (L.) Spreng [205,206]. Other antimicrobial principles are oleanane triterpenes such as germanicol caffeoyl ester (61), camelliagenone (62), and germanicol (63) in B. asiatica (Table S2) [207] or lupeol (40) (Table S2) [208]. These are mainly lipophilic, where activities in non-polar extracts as exemplified with the petroleum ether extract of the stem bark of B. asiatica that strongly restrained B. subtilis with the MIC value of 25 µg/mL, respectively [209]. Other lipophilic to mid-polar principles in B. racemosa are neo-clerodane diterpenes such as nasimalun A (64) [204,208,210]. The aqueous extract suppressed HSV-1 (IC₅₀: 23 µg/mL) [211].

The ethanol extract of the bark (500 µg/disc) of the true mangrove tree Aegiceras corniculatum (L.) Blanco (Aegicerataceae) developed a halo with a broad spectrum of bacteria [28], while the hexane extract of leaves inhibited the growth of Mycobacterium tuberculosis (H₃₇R_v) with the MIC value of 50 µg/mL [212]. The oleanane triterpene acornine 2 (65) isolated from the bark hindered yeasts and filamentous fungi (Table S2) [212]. The ethanol extract of fruits inhibited NDV and SFV [130].

2.4.10. Clade Lamiids

The Lamiids produce various types of antimicrobials (Table S2).

Order Boraginales: The Cordia dichotoma G. Forst. (Boraginaceae) methanol extract restrained S. pyogenes, S. aureus, E. coli, P. aeruginosa, A. niger, and C. albicans [213]. Merrilliodendron megacarpum Sleumer (Icacinaceae) yields the strongly antifungal pyranoindolizinoquinoline alkaloid camptothecin (66) which also restrains a broad spectrum of virus in vitro (Table S2) [214,215,216,217,218,219].

Order Gentianales: Plants in the genus Cerbera L. (Apocynaceae) are antimicrobial. The ethanol extract of Cerbera manghas L. very strongly restrained E. coli and P. aeruginosa (MIC: 4 µg/mL) [17] and VSV (IC₅₀: 0.01 µg/mL) [220]. The methanol extract of seeds of Cerbera odollam Gaertn. developed halos with a broad-spectrum of bacteria [221] and the ethanol extract of fruits suppressed Aspergillus flavus, Fusarium oxysporum, and Penicillium citrum [222]. Note that Apocynaceous indole alkaloids are often antistaphylococcal [223]. The ethanol extract of the leaves (500 µg/well) of Hoya parasitica (Roxb.) Wall. ex Wight (Asclepiadaceae) inhibited the growth of S. aureus, Proteus sp., E. coli, and S. sonnei, and Shigella dysenteriae with the IZD of 23, 19, 10, 8, and 20 mm, respectively [224].

In the Rubiaceae, the organic polar and mid-polar extracts of Guettarda speciosa L., Hydnophytum formicarum Jack, Morinda citrifolia L., and Myrmecodia tuberosa Jack, and Guettarda speciosa L. are antibacterial and antifungal [82,225,226,227,228] (Table S2) [81,162,229,230,231]. Plants in this family yield antimicrobial water soluble iridoid glycosides such as in loganic acid (67) from G. speciosa, which strongly repressed HCV [228], and asperuloside (68) from M. citrifolia (Table S2) [77,91,93,220,232,233,234]. Other antimicrobial principles are caffeic acid derivatives including the antiviral 4,5-di-O-caffeoylquinic acid (69) [229,235] as well as 5,4′-dihydroxy-6,7,8,-trimethoxyflavone (70) in Gardenia lucida Roxb. [91,234,236], antimycobacterial monoterpene indole alkaloids [230], the chalcone butein (71) from H. formicarum [22] (Table S2) [88,237], and the anthraquinones damnacanthal (72) and 1,3-dihydroxy-5-methoxy-2,6-bismethoxymethyl-9,10-anthraquinone [233] (Table S2) [81,229,230,232]. (E)-phytol (73) is strongly antimycobacterial [232]. The ethanol extract of M. citrifolia is weakly active with the FMDV [238] and the methanol extract of Psychotria serpens L. with HSV [155]. The essential oil of the latter is strongly bactericidal with S. aureus (MIC/MBC: 39/39 µg/mL) [239].

Order Lamiales: In the family Acanthaceae, the chloroform extract of the leaves of Acanthus ebracteatus Vahl inhibited the growth of B. cereus, S. aureus, P. aeruginosa, and Proteus vulgaris, C. albicans, Aspergillus fumigatus, and A. niger [240]. This true mangrove herb yields the antibacterial 3,5-dimethoxy-4-hydroxy methyl benzoic acid (74), (Z)-4-coumaric acid 4-O-β-D-glucopyranoside (75), and 6-hydroxy-benzoxazolinone (76) (Table S2) [241]. The alcohol extract given to ducklings orally at a dose of 2 g/kg/day for 14 days evoked a decrease in serum hepatitis B surface antigen, AST, ALT, and improved the hepatic cytoarchitecture [242]. The ethanol extract of roots inhibited the replication of the NDV, Vaccinia virus, ECMV, and SFV [130].

Avicennia species (Avicenniaceae) are true mangrove trees yielding broad-spectrum antibacterials [243,244,245] such as the diterpenes excoecarin A (77), ent-16-hydrozy-3-oxo-13-epi-manoyl-oxide (78), ent-15-hydroxy-labda-8(17), 13E-dien-3-one (79), which repressed Rhizopus orizae and A. niger and rhizophorin B with B. subtilis (Table S2) [246]. The ethanol extract of Avicennia alba L. and Avicennia officinalis L. restrained ECMV [130].

Dolichandrone spathacea (Burm. f.) Bedd. (Bignoniaceae) is a true mangrove tree yielding the hydroxycinnamic acid glycoside derivatives decaffeoyl acteoside (80) and verbascoside (81) active against E. faecalis (ATCC 1034) and S. sonnei (Table S2) [247]. Verbascoside (81) very strongly hindered RSV (Table S2) [248].

An extract of the stems and leaves of Myoporum bontioides (Siebold & Zucc.) A. Gray (Myoporaceae) moderately inhibited the growth of F. oxysporum, Pestalotia mangiferae, Thielaviopsis paradoxa, Colletotrichum musae, Alternaria alternata, Mycosphaerella sentina, and Sphaceloma fawcettii [249]. From this plant, the sesquiterpenes myoporumine A (82) and B (83), (-)-epingaione (84), and (–)-dehydroepingaione (85) strongly repressed MRSA (Table S2) [250]. (-)-Epingaione is a strong inhibitor of filamentous fungi [249]. Other antifungal principles in this plant are homomonoterpenes (Table S2) [251]

In the Verbenaceae, Premna odorata Blanco produces the strong antimycobacterial long chain alkane 1-heneicosyl formate (86) (Table S2) [252]. Essential oil of plants in this family like in the Lamiaceae are often antifungal [253]. The methanol extract (200 µg/disc) developed halos with A. niger and Penicillium cyclopium [254,255].

Order Solanales: The ethanol extract of the flowers of Ipomoea pes-caprae (L.) R. Br. (Convolvulaceae) inhibited the growth of S. aureus, B. subtilis, Streptococcus mutans, P. vulgaris, K. pneumoniae, E. coli, A. flavus, A. niger, and Penicillium sp [256]. The methanol extract of the leaves of Solanum viride R. Br. (Solanaceae) was weakly active against S. aureus and C. albicans [257].

2.4.11. Clade Campanulids

The ethanol extract of the roots of Pluchea indica (L.) Less. (Asteraceae) repressed E. coli, B. cereus, Pseudomonas fluorescens, S. aureus, and S. typhimurium [258]. The aqueous extract of leaves inhibited HIV-1 [259]. The aqueous extract of berries of Scaevola taccada (Gaertn.) Roxb. (Goodeniaceae) restrained HIV-1 [259]. The methanol extract of leaves (500 µg/well) evoked halos with V. cholerae, K. pneumoniae, S. typhi, S. sonnei, F. oxysporum, Fusarium solani, Rhizoctonia solani, and Odium monilioides [260]. This coastal shrub yields the strong antifungal furanocoumarin scataccanol (87) as well as 4-formylsyringol (88) (Table S2) [261].

3. Antimicrobial Extracts and Compounds from Mangrove and Mangrove-Associated Plants with the Potential to Be Used for Shrimp Farming

According to Kuete (2010), crude extracts with MIC values less than 100 µg/mL are antimicrobial [10]. Here, we define a very strongly active extract with a MIC value below 10 µg/mL. An isolated compound is defined as very strongly active for a MIC value below or equal to 1 µg/mL (as well as less than 1 µg/thin layer chromatography), strongly antibacterial (or antifungal) for a MIC value above 1 µg/mL and equal to or below 50 µg/mL, moderately antibacterial (or antifungal) for a MIC from 50 and below 100 µg/mL, weakly antibacterial (or antifungal) for a MIC from 100 and below 500 µg/mL, very weakly antibacterial (or antifungal) for a MIC ranging from 500 to below 2500 µg/mL, and inactive for a MIC value above 2500 µg/mL.

For antiviral principles, we suggest that a compound with an IC₅₀ value below or equal to 1 µg/mL is very strongly active, for an IC₅₀ value above 1 and equal to or below 20 µg/mL strongly antiviral, for an IC₅₀ above 20 and below or equal to 100 µg/mL moderately antiviral, for an IC₅₀ above 100 and below or equal to 500 µg/mL weakly antiviral, for an IC₅₀ ranging from above 500 to below or equal to 2500 µg/mL very weakly antiviral, and inactive with an IC₅₀ value above 2500 µg/mL.

Using these criteria, the strongest antimicrobial extracts from mangrove and mangrove-associated plants that could be of value for shrimp farming are from C. inophyllum (S. aureus, T. rubrum) [63], T. catappa (E. faecalis) [129]., C. manghas (E. coli, P. aeruginosa, VSV) [17,220], and C. odollam (HSV) [223].

The strongest antimicrobial principles identified from the mangrove and mangrove-associated plants that could be of value for shrimp farming are as follows (Figure 1):

(i) Antibacterial: Lupinifolin (35) (Gram-positive and Gram-negative) [116]; 7-hydroxycadalene (46) [152].

(ii) Antifungal: Lupinifolin (35) (Yeasts) [116].

(iii) Antiviral: Naringenin (9) [50], verbascoside (81) [248], inophyllum B (15) [61], 12-deoxyphorbol 13-(3E,5E-decadienoate) (18) [69], 5β-carboxymethyl-3α-hydroxy-2β-hydroxymethyl-1- methylpyrrolidine (19) [70], deguelin (33) [117], deoxypodophyllotoxin (3) [25,116] (9R,10R, 23R)-21,23:23,27-diepoxycycloarta-1,24-diene-3,27-dione (49) [156], gallic acid (21) [83], and 4,5-di-O-caffeoylquinic acid (69).

(iv) We note that most of these principles are hydrophilic or amphiphilic (Figure 1).

4. Spectrum of Activity of Antimicrobial Extracts and Principles from Mangrove and Mangrove-Associated Plants

The following observations can be made:

• (i). No reports on the only lycopod associated with mangrove are available.

• (ii). Of the 26 ferns, nine had antibacterial effects and six are antifungal, and no antiviral activities were reported. The only antimicrobial principle from ferns thus far is the strong antibacterial (Gram-positive) stenopalustroside A [13] (Table 1).

• (iii). The cycad associated with mangroves has antibacterial effects.

• (iv). No reports on the only pine tree associated with mangrove are available.

• (v). Of the 51 monocots, 11 displayed antimicrobial effects, of which eight had antibacterial activity, six with antiviral activity, and none reported with antiviral properties. Active principles isolated were phenolics such as the flavanol naringenin (9) in the Pandanaceae, antibacterial, antifungal, and antiviral orchidaceous phenanthrenes as well as the flavones and antifungal hydroxycinnamic acid of Poaceae (Table 2)

• (vi). Of the 207 dicots, 92 had antimicrobial effects including 78 antibacterial, 39 antifungal, and 25 antiviral effects. A total of about 80 antimicrobial principles were isolated (Table S2).

• (vii). Aqueous and organic polar extracts of plants from the mangrove presented activity against Gram-positive and Gram-negative bacteria, filamentous fungi and yeasts, enveloped and non-enveloped viruses, DNA, and RNA viruses (Table S2).

• (viii). The extract of P. pinnata [262] and gallic acid (21) abounds notably in the true mangrove trees Rhizophora apiculata Bl. and Aegiceras corniculatum (L.) Blanco is a protected shrimp against WSSV [84] as well as an aqueous extract of the true mangrove tree C. tagal (Perr.) C.B. Rob. [263]

5. Medicinal Use of Mangrove and Mangrove-Associated Plants

One could suggest the use of medicinal plants as a more sustainable alternative to chemotherapy in paenid aquaculture. Therefore, the possible beneficial effect of mangrove and mangrove-associated plants for the sanitation of shrimp farms is reinforced by the observation that 85 plants were used for the treatment of infectious diseases including mainly diarrhea, dysentery, and wounds [264,265,266,267,268,269,270,271,272,273,274,275,276,277,278,279,280,281,282,283,284,285,286,287,288,289,290,291,292,293,294] (Table S1). The pharmacological effect of these plants involves active principles that are potentially able to act on paenids, which could be examined further.

6. Mangrove and Mangrove-Associate Plants as Remediation of Shrimp Farming?

Shrimp and prawn farms are regularly affected by (+)-RNA viruses such as the Taura syndrome virus, Yellow head virus, and Gill-associated virus as well as DNA viruses (WSSV, Monodon Baculovirus) and Gram-negative bacteria such as Hepatobacterium penaei and Vibrio spp. [295]. Synthetic drugs are being used in an attempt to evade economic losses but threaten the environment and contribute to the selection of multidrug-resistant pathogenic microorganisms. Being able to produce antimicrobial principles (some of them water soluble like ellagic acid), mangrove and mangrove-associated plants could be used as a source of natural agents and/or afford ecological systems to combat the infections with shrimps and prawns. Polar organic and aqueous extracts of most mangrove and mangrove-associated plants exhibit broad-spectrum antibacterial, antifungal, or antiviral properties in vitro, suggesting that antimicrobial secondary metabolites from plants and plant litter in the sea and brackish waters could afford some control against the overgrowth of pathogenic microbes. Of note, P. pinnata ethanol extract of leaves given to Penaeus monodon as part of feed at the dose of 300 μg/g of body weight/day evoked some levels of protection against WSSV [262]. Gallic acid (21), which abounds notably in the true mangrove trees R. apiculata and A. corniculatum is strongly antiviral and protected shrimps against WSSV [84]. Gallic acid (21) may, at least in part, account for the fact the aqueous extract of the true mangrove tree C. tagal given at the dose of 10% of the body weight, twice a day, protected shrimps against WSSV [263]. Furthermore, gallic acid (21) decreases microbial proliferation in mangrove soil [296] as well as the growth of microalgae [297], which contribute to a decreased production in shrimp aquaculture [298], at least in part, to the alteration in the shrimp’s immune system [299]. The control of pathogenic bacteria may have some beneficial effects for the symbiotic bacteria of shrimp against pathogenic microorganisms [300]. Furthermore, phenolic acids from mangrove and mangrove-associated plants could, by chelation, protect shrimps against toxic metals including cadmium [301,302]. Therefore, it is possible to extend the protective effect of mangrove and mangrove-associated plants to fisheries and crab farming, the latter being affected by Vibrio species [165]. Another interesting feature of mangrove plants is that they are a host for microorganisms for Actinomyces producing antibacterial principles [303].

7. Conclusions

Plants from the Mangroves of Asia and the Pacific produce a vast array of antimicrobial secondary metabolites that could be further examined for their possible development into medications to control microbial outbreaks in aquaculture. In parallel, growing plant mangroves in aquacultures and promoting mangrove-associated aquaculture could be beneficial. The rise in the global population and the imperative to supply shrimps, prawns, crabs, and fish globally requires the preservation of mangroves.

Author Contributions

Conceptualization, C.W., M.S. (Mazdida Sulaiman), and V.N.; Methodology, C.W.; Validation, M.R. (Mohammed Rahmatullah), M.R. (Mogana Rajagopal), A.K.P. and V.N.; Formal analysis, M.S. (Mazdida Sulaiman) and M.S. (Monica Suleiman); Investigation, J.S.S.S. and N.A.R.; Resources, C.W.; Writing—original draft preparation, C.W. and M.Sulaiman; Writing—review and editing, V.N., M.R. (Mohammed Rahmatullah), A.K.P., M.R. (Mogana Rajagopal), M.R. (Mohammed Rahmatullah), N.A.R., J.S.S.S., C.W., Z.A.Z. and M.S. (Monica Suleiman); Visualization, M.S. (Mazdida Sulaiman) and C.W.; Supervision, C.W.; Project administration, C.W.; Funding acquisition, C.W. All authors have read and agreed to the published version of the manuscript.

Institutional Review Board Statement

Not applicable.

Data Availability Statement

Not applicable.

Acknowledgments

Not applicable.

Conflicts of Interest

The authors declare no conflict of interest.

Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Figure and Tables

Figure 1. Natural products from mangrove plants with very strong antimicrobial activities.

Table 1

Ferns and cycads from the mangroves, tidal rivers, and the seashores of Asia and the Pacific with antibacterial and/or antifungal activity.

FAMILYGenus, Species	Extract		Secondary Metabolite Identified
	Antibacterial	Antifungal
SUBCLASS POLYPODIIDAE			Antibacterial: Stenopalustroside A (1), S. epidermidis (MIC = 2 µg/mL) [13].
BLECHNACEAEStenochlaena palustris (Burm. f.) Bedd.	+	+
NEPHROLEPIDACEAENephrolepis biserrata (Sw.) Schott	+	+
POLYPODIACEAEDrynaria quercifolia (L.) J. Sm.	+	+
Drymoglossum piloselloides (L.) Presl.	+	+
Microsorum punctatum (L.) Copel.	+	+
Platycerium coronarium (O.F. Müll.) Desv.	+
Pyrrosia piloselloides (L.) M.G. Price)	+	+
PTERIDACEAEAcrostichum aureum L.	+	+
Acrostichum speciosum Willd.	+
SUBCLASS CYCADIIDAE
CYCADACEAECycas rumphii Miq.	+

Bold: true mangrove plants [3]. +: Activity of extract(s) reported in the literature.

Table 2

Monocots from the mangroves, tidal rivers, and the seashores of the Asia and the Pacific with antibacterial, antifungal, and/or antiviral activity.

FAMILYGenus, Species(Synonym)	Extracts			Antimicrobial Principle(s)
	Antibacterial	Antifungal	Antiviral
ARACEAELasia spinosa (L.) Thwaites	+	+		Antibacterial: Meridinol (7) (100 µg/disc) [47].Antifungal: Meridinol (7) (100 µg/disc) [47].
ARECACEAEPhoenix paludosa Roxb.	+	+		Antibacterial:3′-Acetoxy-6,7-dimetoxy-4′ (2″,3″,4″,6″- tetraacetylglucopyranosyl)flavone (10), P. aeruginosa, E. coli, S flexneri, MIC= 8, 4, and 8 µg/mL, respectively [47]. Tricin (8), P. aeruginosa, E. coli, S. flexneri, MIC = 4, 2, and 2 µg/mL, respectively [47]. Cinnamic acid (11), P. aeruginosa, E. coli, S. flexneri, MIC = 64, 16, and 16µg/mL, respectively [47].Antifungal: 3′-Acetoxy-6,7-dimetoxy-4′ (2″,3″,4″,6″- tetraacetylglucopyranosyl)flavone (10): C. neoformans, C. albicans, C. parapsilosis, MIC: of 16, 8, and 8 µg/mL, respectively [47].Tricin (8), C. neoformans, C. albicans, C. parapsilosis, MIC = 8, 4, and 4 µg/mL, respectively [47].Cinnamic acid (11), C. neoformans, C. albicans, C. parapsilosis, MIC = 64, 32, and 32 µg/mL, respectively [47].
Saribus rotundifolius (Lam.) Bl.	+	+
CYPERACEAECyperus scariosus R. Br.		+
Eleocharis dulcis (Burm. f.) Trin. ex Hensch	+
Rhynchospora corymbosa (L.) Britton
FLAGELLARIACEAEFlagellaria indica L.	+	+		Antiviral: Tricin (8), IVA, IC50 = 4.6 µM, HIV-1, IC50 = 14.4 µg/mL [49].
ORCHIDACEAEAerides odoratum Reinw. ex Bl.	+
Cymbidium finlaysonianum Wall. ex Lindl.		+		Antibacterial: Batatasin III (4), S. aureus, B. subtilis, MRSA, MIC = 250, 500, and 500 µg/mL, respectively [43].Antifungal: Batatasin III (4), A. brassicicola, P. parasitica, C. capsici, B. oryzae, D.medusaea, C. paradoxa moreau, E.turcicum, P. theae, A. citri [44].Antiviral: Batatasin III (4), HSV-1, HSV-2, IC50 = 341.5 and 384.2 µM, respectively [45]. Gigantol (5), HSV-1 and HSV-2, IC50 = 304.1 and 319.3 µM, respectively [45].
Dendrobium moschatum (Buch. -Ham.) Sw.				Antibacterial: Moscatin (6), V. parahemolyticus, S. gallinarum,S. aureus, S. agalactiae, E. faecalis, B. subtilis, R. anatipestifer, MIC = 96, 72, 72, 48, 96, 72, and 72 µg/mL, respectively [46].
PANDANACEAENypa fruticans Wurmb.	+			Antiviral: Naringenin (9), SARS-CoV, 65.2 µM [51]; YFV, EC50: 0.001 M; ZKV [50]
Pandanus tectorius Parkinson
POACEAEPhragmites vallatoria Veldkamp	+	+
RUPPIACEAERuppia maritima L.	+

+: Activity of extract(s) reported in the literature.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/md20100643/s1, Figure S1: Natural products from the plants of the mangroves, tidal rivers, and the seashores of Asia and the Pacific; Table S1: Plants from the mangroves, tidal rivers, and the seashores of Asia and the Pacific, Table S2: Antimicrobial activity of extracts and isolates from the Dicotyledons from the mangroves, tidal rivers, and the seashores of Asia and the Pacific.

References

1. Lightner, D.V.; Redman, R.M.; Pantoja, C.R.; Tang, K.F.J.; Noble, B.L.; Schofield, P.; Mohney, L.L.; Nunan, L.M.; Navarro, S.A. Historic emergence, impact and current status of shrimp pathogens in the Americas. J. Invertebr. Pathol.; 2012; 110, pp. 174-183. [DOI: https://dx.doi.org/10.1016/j.jip.2012.03.006]

2. Thornber, K.; Verner-Jeffreys, D.; Hinchliffe, S.; Rahman, M.M.; Bass, D.; Tyler, C.R. Evaluating antimicrobial resistance in the global shrimp industry. Rev. Aquacult.; 2020; 12, pp. 966-986. [DOI: https://dx.doi.org/10.1111/raq.12367]

3. Giesen, W.; Wulfraat, S.; Zieren, M.; Scholten, L. Mangrove Guidebook for Southeast Asia; FAO: Bangkok, Thailand, Wetlands International: Wageningen, The Netherlands, 2007.

4. Ricklefs, R.E.; Latham, R.E. Global patterns of diversity in mangrove floras. Species Diversity in Ecological Communities: Historical and Geographical Perspectives; University of Chicago Press: Chicago, IL, USA, 1993; pp. 215-229.

5. Stewart, M.; Fairfull, S. Mangroves. Industries; NDOP, . NSW Government: Parramatta, Sydney, 2008.

6. Polidoro, B.A.; Carpenter, K.E.; Collins, L.; Duke, N.C.; Ellison, A.M.; Ellison, J.C.; Farnsworth, E.J.; Fernando, E.S.; Kathiresan, K.; Koedam, N.E. et al. The loss of species: Mangrove extinction risk and geographic areas of global concern. PLoS ONE; 2010; 5, e10095. [DOI: https://dx.doi.org/10.1371/journal.pone.0010095] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/20386710]

7. Rafael, A.; Calumpong, H.P. Fungal infections of mangroves in natural forests and reforestation sites from Philippines. Aquacul Aquar. Conserv. Legisl.; 2019; 12, pp. 2062-2074.

8. Tiku, A.R. Antimicrobial compounds (phytoanticipins and phytoalexins) and their role in plant defense. Co-Evolution of Secondary Metabolites; Springer: Cham, Switzerland, 2020.

9. Wang, Z.; Li, S.; Ge, S.; Lin, S. Review of distribution, extraction methods, and health benefits of bound phenolics in food plants. J. Agric. Food Chem.; 2020; 68, pp. 3330-3343. [DOI: https://dx.doi.org/10.1021/acs.jafc.9b06574] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/32092268]

10. Kuete, V. Potential of Cameroonian plants and derived products against microbial infections: A review. Planta Med.; 2010; 76, pp. 1479-1491. [DOI: https://dx.doi.org/10.1055/s-0030-1250027] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/20533165]

11. Colette, M.; Guentas, L.; Gunkel-Grillon, P.; Callac, N.; Della Patrona, L. Is halophyte species growing in the vicinity of the shrimp ponds a promising agri-aquaculture system for shrimp ponds remediation in New Caledonia?. Marine Pollution Bull.; 2022; 177, 13563. [DOI: https://dx.doi.org/10.1016/j.marpolbul.2022.113563]

12. Zuraini, Z.; Sasidharan, S.; Kaur, S.R.; Nithiyayini, M. Antimicrobial and antifungal activities of local edible fern Stenochlaena palustris (Burm. F.) Bedd. Pharmacol.Online; 2010; 1, pp. 233-237.

13. Liu, H.; Orjala, J.; Sticher, O.; Rali, T. Acylated flavonol glycosides from leaves of Stenochlaena palustris. J. Nat. Prod.; 1999; 62, pp. 70-75. [DOI: https://dx.doi.org/10.1021/np980179f] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/9917285]

14. Padhy, R.; Dash, S.K. Antibacterial evaluation of methanolic Rhizome extract from an in vivo and in vitro grown Pteridophyte, Drynaria quercifolia (Linn.) J. Smith. Asian J. Pharm. Clin. Res.; 2015; 8, pp. 130-138.

15. Amoroso, V.B.; Antesa, D.A.; Buenavista, D.P.; Coritico, F.P. Antimicrobial, antipyretic, and anti-inflammatory activities of selected Philippine medicinal pteridophytes. Asian J. Biodivers.; 2014; 5, 1. [DOI: https://dx.doi.org/10.7828/ajob.v5i1.479]

16. Somchit, M.N.; Hassan, H.; Zuraini, A.; Chong, L.C.; Mohamed, Z.; Zakaria, Z.A. In vitro anti-fungal and anti-bacterial activity of Drymoglossum piloselloides L. Presl. against several fungi responsible for athletes foot and common pathogenic bacteria. Afr. J. Microbiol. Res.; 2011; 5, pp. 3537-3541.

17. Frankova, A.; Vistejnova, L.; Merinas-Amo, T.; Leheckova, Z.; Doskocil, I.; Soon, J.W.; Kudera, T.; Laupua, F.; Alonso-Moraga, A.; Kokoska, L. In vitro antibacterial activity of extracts from Samoan medicinal plants and their effect on proliferation and migration of human fibroblasts. J. Ethnopharmacol.; 2021; 264, 113220. [DOI: https://dx.doi.org/10.1016/j.jep.2020.113220]

18. Desnilasari, D.; Iwansyah, A.C.; Fauziah, R. From local wisdom: Preliminary antibacterial activity of “Tanduk rusa” Fern (Platycerium coronarium). Proceedings of the 1st International Conference on Appropriate Technology Development 2015; Bandung, Indonesia, 5–7 October 2015.

19. Thomas, T. In vitro evaluation of antibacterial activity of Acrostichum aureum Linn. Ind. J. Nat. Prod.; 2012; 3, pp. 135-138.

20. Shamsuddin, A.A.; Najiah, M.; Suvik, A.; Azariyah, M.N.; Kamaruzzaman, B.Y.; Effendy, A.W.; John, B.A. Antibacterial properties of selected mangrove plants against Vibrio species and its cytotoxicity against Artemia salina. World Appl. Sci. J.; 2013; 25, pp. 333-340.

21. Saad, S.; Taher, M.; Susanti, D.; Qaralleh, H.; Awang, A.F.I.B. In vitro antimicrobial activity of mangrove plant Sonneratia alba. Asian Pacific J. Trop. Biomed.; 2012; 2, pp. 427-429. [DOI: https://dx.doi.org/10.1016/S2221-1691(12)60069-0]

22. Khan, A.V.; Ahmed, Q.U.; Khan, A.A.; Shukla, I. Antibacterial activity of Cycas rumphii Miq. leaves extracts against some tropical human pathogenic bacteria. Res. J. Microbiol.; 2011; 6, 761. [DOI: https://dx.doi.org/10.3923/jm.2011.761.768]

23. Amin, E. Phytochemical content and biological activity of the genus Cycas, Family Cycadaceae: A review. Pharm. Sci. Asia; 2021; 4, pp. 300-319.

24. Puvanendran, S.; Wickramasinghe, A.; Karunaratne, D.N.; Carr, G.; Wijesundara, D.S.A.; Andersen, R.; Karunaratne, V. Antioxidant constituents from Xylopia championii. Pharm. Biol.; 2008; 46, pp. 352-355. [DOI: https://dx.doi.org/10.1080/13880200801887989]

25. Sudo, K.; Konno, K.; Shigeta, S.; Yokota, T. Inhibitory effects of podophyllotoxin derivatives on herpes simplex virus replication. Antiv. Chem. Chemothery; 1998; 9, pp. 263-267. [DOI: https://dx.doi.org/10.1177/095632029800900307]

26. Padmaja, V.; Thankamany, V.; Hara, N.; Fujimoto, Y.; Hisham, A. Biological activities of Annona glabra. J. Ethnopharmacol.; 1995; 48, pp. 21-24. [DOI: https://dx.doi.org/10.1016/0378-8741(95)01277-K]

27. Uddin, S.J.; Rouf, R.; Shilpi, J.A.; Alamgir, M.; Nahar, L.; Sarker, S.D. Screening of some Bangladeshi medicinal plants for in vitro antibacterial activity. Orient. Pharm. Exp. Med.; 2008; 8, pp. 316-321. [DOI: https://dx.doi.org/10.3742/OPEM.2008.8.3.316]

28. Goshwami, D.; Rahman, M.M.; Muhit, M.A.; Islam, M.S.; Anasri, M. Antioxidant property, cytotoxicity and antimicrobial activity of Lasia spinosa leaves. Nepal J. Sci. Technol.; 2012; 13, pp. 215-218. [DOI: https://dx.doi.org/10.3126/njst.v13i2.7739]

29. Mondal, B.; Hore, M.; Baishakhi, F.S.; Ramproshad, S.; Sadhu, S.K. Study of antioxidant, antidiabetic and antibacterial activities of mangrove plant Phoenix paludosa. Asian J. Med. Health Res.; 2018; 3, 12.

30. Paul, S.R.; Sayeed, M.; Hakim, M. Antibacterial and cytotoxic activity of the bark of Phoenix paludosa in different solvents. Jordan J. Biol. Sci.; 2017; 10, pp. 213-217.

31. Essien, E.E.; Antia, B.S.; Etuk, E.I. Phytoconstituents, antioxidant and antimicrobial activities of Livistona chinensis (Jacquin), Saribus rotundifolius (Lam.) Blume and Areca catechu Linnaeus Nuts. Pharm. Biosci. J.; 2017; 10, pp. 59-67. [DOI: https://dx.doi.org/10.20510/ukjpb/5/i1/147026]

32. Khan, W.U.; Khan, R.A.; Ahmed, M.; Khan, L.U.; Khan, M.W. Pharmacological evaluation of methanolic extract of Cyperus scariosus. Bangladesh J. Pharmacol.; 2016; 11, pp. 353-358. [DOI: https://dx.doi.org/10.3329/bjp.v11i2.23611]

33. Zhan, G.; Pan, L.Q.; Mao, S.B.; Zhang, W.; Wei, Y.Y.; Tu, K. Study on antibacterial properties and major bioactive constituents of Chinese water chestnut (Eleocharis dulcis) peels extracts/fractions. Eur. Food Res. Technol.; 2014; 238, pp. 789-796. [DOI: https://dx.doi.org/10.1007/s00217-013-2151-2]

34. Ramadhani, D.A.; Novita, H.; Rajamuddin, M.A.L.; Elya, B. Chemical compounds screening of leaves extract from Eleocharis dulcis (Burm. f.) trin. ex hensch and in vitro antibacterial pathogenic test for fish. AACL Bioflux.; 2020; 13, pp. 2770-2778.

35. Ebana, R.U.B.; Etok, C.A.; Edet, U.O. Phytochemical screening and antimicrobial activity of Nypa fruticans harvested from Oporo River in the Niger Delta Region of Nigeria. Int. J. Innov. Appl. Stud.; 2015; 10, 1120.

36. Joshi, B.; Panda, S.K.; Jouneghani, R.S.; Liu, M.; Parajuli, N.; Leyssen, P.; Neyts, J.; Luyten, W. Antibacterial, antifungal, antiviral, and anthelmintic activities of medicinal plants of Nepal selected based on ethnobotanical evidence. Evidence-Based Compl. Alt. Med.; 2020; 2020, pp. 1-13. [DOI: https://dx.doi.org/10.1155/2020/1043471] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/32382275]

37. Bushmann, P.J.; Ailstock, M.S. Antibacterial compounds in estuarine submersed aquatic plants. J. Exp. Marine Biol. Ecol.; 2006; 331, pp. 41-50. [DOI: https://dx.doi.org/10.1016/j.jembe.2005.10.005]

38. Nugraha, A.S.; Permatasari, A.E.N.; Kadarwenny, C.P.; Pratoko, D.K.; Triatmoko, B.; Rosyidi, V.A.; Norcahyanti, I.; Dewi, I.P.; Dianasari, D.; Sary, I.P. et al. Phytochemical screening and the antimicrobial and antioxidant activities of medicinal plants of Meru Betiri National park–Indonesia. J. Herbs Spices Med. Plants; 2020; 26, pp. 303-314. [DOI: https://dx.doi.org/10.1080/10496475.2020.1734136]

39. Klawikkan, N.; Nukoolkarn, V.; Jirakanjanakit, N.; Yoksan, S.; Wiwat, C. Effect of Thai medicinal plant extracts against Dengue virus in vitro. Mahidol Univ. J. Pharm. Sci.; 2011; 38, pp. 13-18.

40. Kaushik, S.; Kaushik, S.; Sharma, V.; Yadav, J. Antiviral and therapeutic uses of medicinal plants and their derivatives against Dengue viruses. Pharm. Rev.; 2018; 12, pp. 13-18.

41. Paul, P.; Chowdhury, A.; Nath, D.; Bhattacharjee, M.K. Antimicrobial efficacy of orchid extracts as potential inhibitors of antibiotic resistant strains of E. coli. Asian J. Pharm. Clin. Res.; 2013; 6, pp. 108-111.

42. Juneja, R.K.; Sharma, S.C.; Tandon, J.S. Two substituted bibenzyls and a dihydrophenanthrene from Cymbidium aloifolium. Phytochemistry; 1987; 26, pp. 1123-1125. [DOI: https://dx.doi.org/10.1016/S0031-9422(00)82362-6]

43. Jiang, S.; Wang, M.; Jiang, L.; Xie, Q.; Yuan, H.; Yang, Y.; Zafar, S.; Liu, Y.; Jian, Y.; Li, B. et al. The medicinal uses of the genus Bletilla in traditional Chinese medicine: A phytochemical and pharmacological review. J. Ethnopharmacol.; 2021; 280, 114263. [DOI: https://dx.doi.org/10.1016/j.jep.2021.114263]

44. Zhou, X.M.; Zheng, C.J.; Gan, L.S.; Chen, G.Y.; Zhang, X.P.; Song, X.P.; Li, G.N.; Sun, C.G. Bioactive phenanthrene and bibenzyl derivatives from the stems of Dendrobium nobile. J. Nat. Prod.; 2016; 79, pp. 1791-1797. [DOI: https://dx.doi.org/10.1021/acs.jnatprod.6b00252]

45. Sukphan, P.; Sritularak, B.; Mekboonsonglarp, W.; Lipipun, V.; Likhitwitayawuid, K. Chemical constituents of Dendrobium venustum and their antimalarial and anti-herpetic properties. Nat. Prod. Commun.; 2014; 9, 1934578X1400900625. [DOI: https://dx.doi.org/10.1177/1934578X1400900625]

46. Ren, J.; Qian, X.P.; Guo, Y.G.; Li, T.; Yan, S.K.; Jin, H.Z.; Zhang, W.D. Two new phenanthrene glycosides from Liparis regnieri Finet and their antibacterial activities. Phytochem. Lett.; 2016; 18, pp. 64-67. [DOI: https://dx.doi.org/10.1016/j.phytol.2016.08.023]

47. Hasan, C.M.; Alam, F.; Haque, M.; Sohrab, M.H.; Monsur, M.A.; Ahmed, N. Antimicrobial and cytotoxic activity from Lasia spinosa and isolated lignan. Lat. Am. J. Pharm.; 2011; 30, pp. 550-553.

48. Pagning, A.L.N.; Lateef, M.; Tapondjou, L.A.; Kuiate, J.R.; Ngnokam, D.; Ali, M.S. New triterpene and new flavone glucoside from Rhynchospora corymbosa (Cyperaceae) with their antimicrobial, tyrosinase and butyrylcholinesterase inhibitory activities. Phytochem. Lett.; 2016; 2016, pp. 121-128. [DOI: https://dx.doi.org/10.1016/j.phytol.2016.03.011]

49. Yazawa, K.; Kurokawa, M.; Obuchi, M.; Li, Y.; Yamada, R.; Sadanari, H.; Matsubara, K.; Watanabe, K.; Koketsu, M.; Tuchida, Y. et al. Anti-influenza virus activity of tricin, 4′, 5, 7-trihydroxy-3′, 5′-dimethoxyflavone. Antiv. Chem. Chemother.; 2011; 22, pp. 1-11. [DOI: https://dx.doi.org/10.3851/IMP1782]

50. Castrillo, M.; Córdova, T.; Cabrera, G.; Rodríguez-Ortega, M. Effect of naringenin, hesperetin and their glycosides forms on the replication of the 17D strain of yellow fever virus. Av. Biomed.; 2015; 4, pp. 69-78.

51. Clementi, N.; Scagnolari, C.; D’Amore, A.; Palombi, F.; Criscuolo, E.; Frasca, F.; Pierangeli, A.; Mancini, N.; Antonelli, G.; Clementi, M. et al. Naringenin is a powerful inhibitor of SARS-CoV-2 infection in vitro. Pharmacol. Res.; 2021; 163, 105255. [DOI: https://dx.doi.org/10.1016/j.phrs.2020.105255]

52. Sari, R.S.E.; Soegianto, L.; Liliek, S. Uji aktivitas antimikroba ekstrak etanol daun Cayratia trifolia terhadap S. aureus dan Candida albicans. J. Farm. Sains Dan Terap.; 2018; 5, pp. 23-29.

53. Nguyen, T.N.A.; Dao, T.T.; Tung, B.T.; Choi, H.; Kim, E.; Park, J.; Lim, S.I.; Oh, W.K. Influenza A (H1N1) neuraminidase inhibitors from Vitis amurensis. Food Chem.; 2011; 124, pp. 437-443. [DOI: https://dx.doi.org/10.1016/j.foodchem.2010.06.049]

54. Lee, S.; Mailar, K.; Kim, M.I.; Park, M.; Kim, J.; Min, D.H.; Heo, T.H.; Bae, S.K.; Choi, W.; Lee, C. Plant-derived purification, chemical synthesis, and in vitro/in vivo evaluation of a resveratrol dimer, viniferin, as an HCV replication inhibitor. Viruses; 2019; 11, 890. [DOI: https://dx.doi.org/10.3390/v11100890]

55. Aguilar-Guadarrama, B.; Navarro, V.; Leon-Rivera, I.; Rios, M.Y. Active compounds against tinea pedis dermatophytes from Ageratina pichinchensis var. bustamenta. Nat. Prod. Res.; 2009; 23, pp. 1559-1565. [DOI: https://dx.doi.org/10.1080/14786410902843301]

56. Sahidin, I.; Wahyuni, W.; Malaka, M.H.; Imran, I. Antibacterial and cytotoxic potencies of stilbene oligomers from stem barks of baoti (Dryobalanops lanceolata) growing in Kendari, Indonesia. Asian J. Pharm. Clin. Res.; 2017; 10, pp. 139-143.

57. Basri, D.F.; Xian, L.W.; Abdul Shukor, N.I.; Latip, J. Bacteriostatic antimicrobial combination: Antagonistic interaction between epsilon-viniferin and vancomycin against methicillin-resistant Staphylococcus aureus. BioMed Res. Int.; 2014; 2014, 461756. [DOI: https://dx.doi.org/10.1155/2014/461756] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/24783205]

58. Yim, N.; Trung, T.N.; Kim, J.P.; Lee, S.; Na, M.; Jung, H.; Kim, H.S.; Kim, Y.H.; Bae, K. The antimicrobial activity of compounds from the leaf and stem of Vitis amurensis against two oral pathogens. Bioorg. Med. Chem. Lett.; 2010; 20, pp. 1165-1168. [DOI: https://dx.doi.org/10.1016/j.bmcl.2009.12.020]

59. Mattio, L.M.; Dallavalle, S.; Musso, L.; Filardi, R.; Franzetti, L.; Pellegrino, L.; D’Incecco, P.; Mora, D.; Pinto, A.; Arioli, S. Antimicrobial activity of resveratrol-derived monomers and dimers against foodborne pathogens. Sci. Rep.; 2019; 9, 7843. [DOI: https://dx.doi.org/10.1038/s41598-019-55975-1]

60. Yimdjo, M.C.; Azebaze, A.G.; Nkengfack, A.E.; Meyer, A.M.; Bodo, B.; Fomum, Z.T. Antimicrobial and cytotoxic agents from Calophyllum inophyllum. Phytochemistry; 2004; 65, pp. 2789-2795. [DOI: https://dx.doi.org/10.1016/j.phytochem.2004.08.024]

61. Patil, A.D.; Freyer, A.J.; Eggleston, D.S.; Haltiwanger, R.C.; Bean, M.F.; Taylor, P.B.; Caranfa, M.J.; Breen, A.L.; Bartus, H.R. The inophyllums, novel inhibitors of HIV-1 reverse transcriptase isolated from the Malaysian tree, Calophyllum inophyllum Linn. J. Med. Chem.; 1993; 36, pp. 4131-4138. [DOI: https://dx.doi.org/10.1021/jm00078a001]

62. Hamdillah, A.; Isnansetyo, A.; Istiqomah, I.; Puspita, I.D.; Handayani, D.P.; Kaneko, T. Antibacterial activity of coastal plants and marine sponges from Kei Island Indonesia against bacterial fish pathogens. Pharmacog. J.; 2019; 11, pp. 812-817. [DOI: https://dx.doi.org/10.5530/pj.2019.11.130]

63. Cuesta-Rubio, O.; Oubada, A.; Bello, A.; Maes, L.; Cos, P.; Monzote, L. Antimicrobial assessment of resins from Calophyllum antillanum and Calophyllum inophyllum. Phytother. Res.; 2015; 29, pp. 1991-1994. [DOI: https://dx.doi.org/10.1002/ptr.5506] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/26514875]

64. Spino, C.; Dodier, M.; Sotheeswaran, S. Anti-HIV coumarins from Calophyllum seed oil. Bioorg. Med. Chem. Lett.; 1998; 8, pp. 475-3478. [DOI: https://dx.doi.org/10.1016/S0960-894X(98)00628-3]

65. Agoramoorthy, G.; Chandrasekaran, M.; Venkatesalu, V.; Hsu, M.J. Antibacterial and antifungal activities of fatty acid methyl esters of the blind-your-eye mangrove from India. Braz. J. Microbiol.; 2007; 38, pp. 739-742. [DOI: https://dx.doi.org/10.1590/S1517-83822007000400028]

66. Ravikumar, S.; Gnanadesigan, M.; Vijayakumar, V. In vitro antibacterial activity of diterpene and benzoxazole derivatives from Excoecaria agallocha L. Int. J. Biol. Chem. Sci.; 2010; 4, pp. 692-701.

67. Sabu, K.R.; Sugathan, S.; Idhayadhulla, A.; Woldemariam, M.; Aklilu, A.; Biresaw, G.; Tsegaye, B.; Manilal, A. Antibacterial, antifungal, and cytotoxic activity of Excoecaria agallocha leaf extract. J. Exp. Pharmacol.; 2022; 14, pp. 692-707.

68. Premanathan, M.; Rajendran, S.; Ramanathan, T.; Kathiresan, K. A survey of some Indian medicinal plants for anti-human immunodeficiency virus (HIV) activity. Indian. J. Med. Res.; 2000; 112, 73. [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/11094851]

69. Erickson, K.L.; Beutler, J.A.; Cardellina, J.H.; McMahon, J.B.; Newman, D.J.; Boyd, M.R. A novel phorbol ester from Excoecaria agallocha. J. Nat. Prod.; 1995; 58, pp. 769-772. [DOI: https://dx.doi.org/10.1021/np50119a020]

70. Yan, R.Y.; Wang, H.Q.; Liu, C.; Chen, R.Y.; Yu, D.Q. Three new water-soluble alkaloids from the leaves of Suregada glomerulata (Blume) Baill. Fitoter; 2011; 82, pp. 247-250. [DOI: https://dx.doi.org/10.1016/j.fitote.2010.10.004] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/20940031]

71. Millat, M.S.; Islam, S.; Hussain, M.S.; Moghal, M.M.R.; Islam, T. Antibacterial profiling of Launaea sarmentosa (Willd.) and Bruguiera cylindrica (L.): Two distinct ethno medicinal plants of Bangladesh. Eur. Exp. Biol.; 2017; 7, pp. 1-5.

72. Bibi Sadeer, N.; Haddad, J.G.; Oday Ezzat, M.; Desprès, P.; Abdallah, H.H.; Zengin, G.; Uysal, A.; El Kalamouni, C.; Gallo, M.; Montesano, D. et al. Bruguiera gymnorhiza (L.) Lam. at the forefront of pharma to confront Zika virus and microbial infections—An in vitro and in silico perspective. Molecules; 2021; 26, 5768. [DOI: https://dx.doi.org/10.3390/molecules26195768] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/34641314]

73. Ravikumar, S.; Gnanadesigan, M.; Suganthi, P.; Ramalakshmi, A. Antibacterial potential of chosen mangrove plants against isolated urinary tract infectious bacterial pathogens. Int. J. Med. Sci.; 2010; 2, pp. 94-99.

74. Jasna, T.K.; Khaleel, K.M.; Rajina, M. In vitro antibacterial activity of mangrove plant Kandelia candel (L.) druce (Rhizophoraceae). World J. Pharma Res.; 2017; 6, pp. 470-477.

75. Mahalakshmi, G.; Vengadeshkumar, L.; Rajamohan, K.; Sanjaygandhi, S.; Sharmila, A.M. Leaf extract of Rhizophora apiculata as a potential bio-inducer of early blight disease resistance in tomato plant. Nov. Res. Microbiol. J.; 2020; 4, 714.

76. Burhanuddin, B.; Saru, A.; Rantetondok, A.; Zainuddin, E.N. Antibacterial activity Rhizophora stylosa and Avicennia marina of mangrove fruit extraction on vibriosis of mangrove crab larvae (Scylla serrata Forsskal). Int. J. Environ. Agric. Biotechnol.; 2019; 4, pp. 1242-1248. [DOI: https://dx.doi.org/10.22161/ijeab.4452]

77. Lim, S.H.; Darah, I.; Jain, K. Antimicrobial activities of tannins extracted from Rhizophora apiculata barks. J. Trop. Forest Sci.; 2006; 18, pp. 59-65.

78. Kokpol, U.; Chavasiri, W.; Chittawong, V.; Bruce, M.; Cunningham, G.N.; Miles, D.H. Long chain aliphatic alcohols and saturated carboxylic acids from heartwood of Rhizophora apiculata. Phytochemistry; 1993; 33, pp. 1129-1131. [DOI: https://dx.doi.org/10.1016/0031-9422(93)85036-Q]

79. Thiem, B.; Goślińska, O. Antimicrobial activity of Rubus chamaemorus leaves. Fitoter; 2004; 75, pp. 93-95. [DOI: https://dx.doi.org/10.1016/j.fitote.2003.08.014] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/14693229]

80. Chacha, M.; Mapitse, R.; Afolayan, A.J.; Majinda, R.R. Antibacterial diterpenes from the roots of Ceriops tagal. Nat. Prod. Commun.; 2008; 3, pp. 17-20. [DOI: https://dx.doi.org/10.1177/1934578X0800300104]

81. Fogliani, B.; Raharivelomanana, P.; Bianchini, J.P.; Bouraı, S.; Hnawia, E. Bioactive ellagitannins from Cunonia macrophylla, an endemic Cunoniaceae from New Caledonia. Phytochem.; 2005; 66, pp. 241-247. [DOI: https://dx.doi.org/10.1016/j.phytochem.2004.11.016] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/15652581]

82. Jayaraman, S.K.; Manoharan, M.S.; Illanchezian, S. Antibacterial, antifungal and tumor cell suppression potential of Morinda citrifolia fruit extracts. Int. J. Integr. Biol.; 2008; 3, pp. 44-49.

83. Choi, H.J.; Song, J.H.; Bhatt, L.R.; Baek, S.H. Anti-human rhinovirus activity of gallic acid possessing antioxidant capacity. Phytother. Res.; 2010; 24, pp. 1292-1296. [DOI: https://dx.doi.org/10.1002/ptr.3101] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/20104501]

84. Shan, L.P.; Zhang, X.; Hu, Y.; Liu, L.; Chen, J. Antiviral activity of esculin against white spot syndrome virus: A new starting point for prevention and control of white spot disease outbreaks in shrimp seedling culture. J. Fish Dis.; 2022; 45, pp. 59-68. [DOI: https://dx.doi.org/10.1111/jfd.13533]

85. Hatano, T.; Kusuda, M.; Hori, M.; Shiota, S.; Tsuchiya, T.; Yoshida, T. Theasinensin A, a tea polyphenol formed from Epigallocatechin gallate, suppresses antibiotic resistance of methicillin-resistant S. aureus. Planta Med.; 2003; 69, pp. 984-989. [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/14735433]

86. Xu, T.; Wang, Z.; Lei, T.; Lv, C.; Wang, J.; Lu, J. New flavonoid glycosides from Sedum aizoon L. Fitoter; 2015; 101, pp. 125-132. [DOI: https://dx.doi.org/10.1016/j.fitote.2014.12.014] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/25562804]

87. Hafid, A.F.; Wahyuni, T.S.; Tumewu, L.; Apryani, E.V.H.Y.; Permanasari, A.A.; Adianti, M.; Kawahara, N. Antihepatitis C virus activity of Indonesian Mahogany (Toona Sureni). Asian J. Pharm. Clin. Res.; 2018; 11, pp. 87-90. [DOI: https://dx.doi.org/10.22159/ajpcr.2018.v11i2.18126]

88. Hsu, W.C.; Chang, S.P.; Lin, L.C.; Li, C.L.; Richardson, C.D.; Lin, C.C.; Lin, L.T. Limonium sinense and gallic acid suppress hepatitis C virus infection by blocking early viral entry. Antiv. Res.; 2015; 118, pp. 139-147. [DOI: https://dx.doi.org/10.1016/j.antiviral.2015.04.003]

89. You, H.L.; Huang, C.C.; Chen, C.J.; Chang, C.C.; Liao, P.L.; Huang, S.T. Anti-pandemic influenza A (H1N1) virus potential of catechin and gallic acid. J. Chin. Med. Assoc.; 2018; 81, pp. 458-468. [DOI: https://dx.doi.org/10.1016/j.jcma.2017.11.007] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/29287704]

90. Weng, J.R.; Lin, C.S.; Lai, H.C.; Lin, Y.P.; Wang, C.Y.; Tsai, Y.C.; Wu, K.C.; Huang, S.H.; Lin, C.W. Antiviral activity of Sambucus ormosana Nakai ethanol extract and related phenolic acid constituents against human coronavirus NL63. Virus Res.; 2019; 273, 197767. [DOI: https://dx.doi.org/10.1016/j.virusres.2019.197767] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/31560964]

91. Afifi, F.Ü.; Al-Khalil, S.; Abdul-Haq, B.K.; Mahasneh, A.; Al-Eisawi, D.M.; Sharaf, M.; Wong, L.K.; Schiff, P.L., Jr. Antifungal flavonoids from Varthemia iphionoides. Phytother. Res.; 1991; 5, pp. 173-175. [DOI: https://dx.doi.org/10.1002/ptr.2650050407]

92. Wang, J.; Qin, X.; Chen, Z.; Ju, Z.; He, W.; Tan, Y.; Zhou, X.; Tu, Z.; Lu, F.; Liu, Y. Two new anthraquinones with antiviral activities from the barks of Morinda citrifolia (Noni). Phytochem. Lett.; 2016; 15, pp. 13-15. [DOI: https://dx.doi.org/10.1016/j.phytol.2015.11.006]

93. Saludes, J.P.; Garson, M.J.; Franzblau, S.G.; Aguinaldo, A.M. Antitubercular constituents from the hexane fraction of Morinda citrifolia Linn. (Rubiaceae). Phytother. Res.; 2002; 16, pp. 683-685. [DOI: https://dx.doi.org/10.1002/ptr.1003]

94. Simlai, A.; Mukherjee, K.; Mandal, A.; Bhattacharya, K.; Samanta, A.; Roy, A. Partial purification and characterization of an antimicrobial activity from the wood extract of mangrove plant Ceriops decandra. EXCLI J.; 2016; 15, pp. 103-112.

95. Saeed, M.A.; Sabir, A.W. Antibacterial activity of Caesalpinia bonducella seeds. Fitoter; 2001; 72, pp. 807-809. [DOI: https://dx.doi.org/10.1016/S0367-326X(01)00292-1]

96. Simin, K.; Khaliq-uz-Zaman, S.M.; Ahmad, V.U. Antimicrobial activity of seed extracts and bondenolide from Caesalpinia bonduc (L.) Roxb. Phytother. Res.; 2001; 15, pp. 437-440. [DOI: https://dx.doi.org/10.1002/ptr.756] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/11507739]

97. Arif, T.; Mandal, T.K.; Kumar, N.; Bhosale, J.D.; Hole, A.; Sharma, G.L.; Padhi, M.M.; Lavekar, G.S.; Dabur, R. In vitro and in vivo antimicrobial activities of seeds of Caesalpinia bonduc (Lin.) Roxb. J. Ethnopharmacol.; 2009; 123, pp. 177-180. [DOI: https://dx.doi.org/10.1016/j.jep.2009.02.040] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/19429358]

98. Ata, A.; Udenigwe, C.C.; Gale, E.M.; Samarasekera, R. Minor chemical constituents of Caesalpinia bonduc. Nat. Prod. Commun.; 2009; 4, pp. 311-314. [DOI: https://dx.doi.org/10.1177/1934578X0900400302]

99. Idrus, I.; Kurniawan, F.; Mustapa, F.; Wibowo, D. Concentration Effect of Leaf Extract from Kekara Laut (Canavalia Maritima Thou.) in Inhibiting of Staphylococcus Epidermidis Bacteria With a Statistical Science Approach. Indo. J. Chem. Res.; 2021; 8, pp. 180-185. [DOI: https://dx.doi.org/10.30598//ijcr.2021.8-irm]

100. Powar, P. Antifungal activity of Mangrove bark. Int. J. Pharm. Bio. Sci.; 2011; 4, pp. 484-488.

101. Suhendi, A.; Indrayudha, P.; Azizah, T. Antibacterial activity of ethanol extract of steam bark of Cynometra ramiflora Linn against various bacterial. Open Conf. Proc. J.; 2013; 4, 1. [DOI: https://dx.doi.org/10.2174/2210289201304010092]

102. Kumar, V.A.; Ammani, K.; Siddhardha, B. In vitro antimicrobial activity of leaf extracts of certain mangrove plants collected from Godavari estuarine of Konaseema delta, India. Int. J. Med. Arom. Plants.; 2011; 1, pp. 132-136.

103. Xin, L.Y.; Min, T.H.; Zin, P.N.L.M.; Pulingam, T.; Appaturi, J.N.; Parumasivam, T. Antibacterial potential of Malaysian ethnomedicinal plants against methicillin-susceptible Staphylococcus aureus (MSSA) and methicillin-resistant Staphylococcus aureus (MRSA). Saudi J. Biol.Sci.; 2021; 28, pp. 5884-5889. [DOI: https://dx.doi.org/10.1016/j.sjbs.2021.06.036]

104. Gunasekara, T.D.C.P.; Radhika, N.D.M.; Ragunathan, K.K.; Gunathilaka, D.P.P.; Weerasekera, M.M.; Hewageegana, H.G.S.P.; Arawwawala, L.A.D.M.; Fernando, S.S.N. Determination of antimicrobial potential of five herbs used in ayurveda practices against Candida albicans, Candida parapsilosis and methicillin resistant S. aureus. Anc. Sci. Life.; 2017; 36, 187. [DOI: https://dx.doi.org/10.4103/asl.ASL_179_16]

105. Rattanasuk, S.; Boongapim, R.; Phiwthong, T. Antibacterial activity of Cathormion umbellatum. Bangladesh J. Pharmacol.; 2021; 16, pp. 91-95. [DOI: https://dx.doi.org/10.3329/bjp.v16i3.53420]

106. Hamburger, M.O.; Cordell, G.A.; Tantivatana, P.; Ruangrungsi, N. Traditional medicinal plants of Thailand, VIII. Isoflavonoids of Dalbergia candenatensis. J. Nat. Prod.; 1987; 50, pp. 696-699. [DOI: https://dx.doi.org/10.1021/np50052a020] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/3430167]

107. Sekine, T.; Inagaki, M.; Ikegami, F.; Fujii, Y.; Ruangrungsi, N. Six diprenylisoflavones, derrisisoflavones A–F, from Derris scandens. Phytochemistry; 1999; 52, pp. 87-94. [DOI: https://dx.doi.org/10.1016/S0031-9422(99)00103-X]

108. Hussain, H.; Al-Harrasi, A.; Krohn, K.; Kouam, S.F.; Abbas, G.; Shah, A.; Raees, M.A.; Ullah, R.; Aziz, S.; Schulz, B. Phytochemical investigation and antimicrobial activity of Derris scandens. J. King Saud Univ.-Sci.; 2015; 27, pp. 375-378. [DOI: https://dx.doi.org/10.1016/j.jksus.2015.01.001]

109. Mohotti, S.; Rajendran, S.; Muhammad, T.; Strömstedt, A.A.; Adhikari, A.; Burman, R.; De Silva, E.D.; Göransson, U.; Hettiarachchi, C.M.; Gunasekera, S. Screening for bioactive secondary metabolites in Sri Lankan medicinal plants by microfractionation and targeted isolation of antimicrobial flavonoids from Derris scandens. J. Ethnopharmacol.; 2020; 246, 112158. [DOI: https://dx.doi.org/10.1016/j.jep.2019.112158]

110. Mahabusarakam, W.; Deachathai, S.; Phongpaichit, S.; Jansakul, C.; Taylor, W.C. A benzil and isoflavone derivatives from Derris scandens Benth. Phytochemistry; 2004; 65, pp. 1185-1191. [DOI: https://dx.doi.org/10.1016/j.phytochem.2004.03.006] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/15110702]

111. Mathaiyan, M.; Suresh, A.; Balamurugan, R. Binding property of HIV p24 and reverse transcriptase by chalcones from Pongamia pinnata seeds. Bioinformation; 2018; 14, pp. 279-284. [DOI: https://dx.doi.org/10.6026/97320630014279] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/30237673]

112. Nukui, M.; O’Connor, C.M.; Murphy, E.A. The natural flavonoid compound deguelin inhibits HCMV lytic replication within fibroblasts. Viruses; 2018; 10, 614. [DOI: https://dx.doi.org/10.3390/v10110614]

113. Yusuf, A.I.; Dewi, B.E.; Sjatha, F. Antiviral activity of Cynometra ramiflora Linn leaves extract against replication of Dengue virus serotype 2 on Huh 7.5 cell in vitro. Proceedings of the BROMO Conference (BROMO 2018)—Symposium on Natural Product and Biodiversity; Surabaya, Indonesia, 11–12 July 2018; pp. 1-4.

114. Takatsuki, A.; Nakatani, N.; Morimoto, M.; Tamura, G.; Matsui, M.; Arima, K.; Yamaguchi, I.; Misato, T. Antiviral and antitumor antibiotics. XX. Effects of rotenone, deguelin, and related compounds on animal and plant viruses. Appl. Microbiol.; 1969; 18, pp. 660-667. [DOI: https://dx.doi.org/10.1128/am.18.4.660-667.1969]

115. Yusook, K.; Weeranantanapan, O.; Hua, Y.; Kumkrai, P.; Chudapongse, N. Lupinifolin from Derris reticulata possesses bactericidal activity on S. aureus by disrupting bacterial cell membrane. J. Nat. Med.; 2017; 71, pp. 357-366. [DOI: https://dx.doi.org/10.1007/s11418-016-1065-2]

116. Mazimba, O.; Masesane, I.B.; Majinda, R.R. A flavanone and antimicrobial activities of the constituents of extracts from Mundulea sericea. Nat. Prod. Res.; 2012; 26, pp. 1817-1823. [DOI: https://dx.doi.org/10.1080/14786419.2011.616504]

117. Phrutivorapongkul, A.; Lipipun, V.; Ruangrungsi, N.; Watanabe, T.; Ishikawa, T. Studies on the constituents of seeds of Pachyrrhizus erosus and their anti herpes simplex virus (HSV) activities. Chem. Pharm. Bull.; 2002; 50, pp. 534-537. [DOI: https://dx.doi.org/10.1248/cpb.50.534] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/11964004]

118. Nehad, M.G.; Abdulrahaman, S.H. Antimicrobial efficacy of Casuarina equisetifolia extracts against some pathogenic microorganisms. J. Med. Plants Res.; 2012; 6, pp. 5819-5825.

119. Lagnika, L.; Amoussa, A.M.O.; Oketokoun, S.A.; Adjovi, Y.; Sanni, A. In vitro antifungal and antioxidant activities of two Benin medicinal plants. J. Med. Plants Res.; 2014; 8, pp. 513-519.

120. Kumar, U.M.N.; Panneerselvam, T. Efficacy of aqueous and ethanol extracts Casuarina equisetifolia for potential antimicrobial activity. World J. Pharm. Pharm. Sci.; 2015; 4, pp. 1877-1882.

121. Ao, C.; Li, A.; Elzaawely, A.A.; Xuan, T.D.; Tawata, S. Evaluation of antioxidant and antibacterial activities of Ficus microcarpa L. fil. extract. Food Control; 2008; 19, pp. 940-948. [DOI: https://dx.doi.org/10.1016/j.foodcont.2007.09.007]

122. Hu, Y.; Wu, X.; Liu, N.; Zhang, F.; Lu, Y.; Zhang, Y.; Fu, L. Flavans with anti-HSV activity from the leaves of Ficus microcarpa L. J. Trop. Subtrop. Bot.; 2010; 18, pp. 559-563.

123. Nantachit, K.; Sirilun, S.; Nobsathian, S.; Rungjang, S. Three new polycyclic containing sulfur compounds from the seeds of Combretum quadrangulare kurz (Combretaceae), antifungal and anti-mycobacterium activities. Chiang Mai J. Sci.; 2017; 44, pp. 157-167.

124. Pawar, S.P.; Pal, S.C. Antimicrobial activity of extracts of Terminalia catappa root. Indian J Med. Sci.; 2002; 56, pp. 276-278.

125. Terças, A.G.; Monteiro, A.D.S.; Moffa, E.B.; Dos Santos, J.R.; Sousa, E.M.D.; Pinto, A.R.; Costa, P.C.; Borges, A.C.; Torres, L.; Barros Filho, A.K. et al. Phytochemical characterization of Terminalia catappa linn. extracts and their antifungal activities against candida spp. Front. Microbiol.; 2017; 8, 595. [DOI: https://dx.doi.org/10.3389/fmicb.2017.00595]

126. Adesina, S.K.; Idowu, O.; Ogundaini, A.O.; Oladimeji, H.; Olugbade, T.A.; Onawunmi, G.O.; Pais, M. Antimicrobial constituents of the leaves of Acalypha wilkesiana and Acalypha hispida. Phytother. Res.; 2000; 14, pp. 371-374. [DOI: https://dx.doi.org/10.1002/1099-1573(200008)14:5<371::AID-PTR625>3.0.CO;2-F]

127. Yeo, S.G.; Song, J.H.; Hong, E.H.; Lee, B.R.; Kwon, Y.S.; Chang, S.Y.; Kim, S.H.; Won Lee, S.; Park, J.H.; Ko, H.J. Antiviral effects of Phyllanthus urinaria containing corilagin against human enterovirus 71 and Coxsackievirus A16 in vitro. Arch. Pharm. Res.; 2015; 38, pp. 193-202. [DOI: https://dx.doi.org/10.1007/s12272-014-0390-9] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/24752860]

128. Dao, N.T.; Jang, Y.; Kim, M.; Nguyen, H.H.; Pham, D.Q.; Le Dang, Q.; Van Nguyen, M.; Yun, B.S.; Pham, Q.M.; Kim, J.C. et al. Chemical constituents and anti-influenza viral activity of the leaves of Vietnamese plant Elaeocarpus tonkinensis. Rec. Nat. Prod.; 2019; 13, pp. 71-80. [DOI: https://dx.doi.org/10.25135/rnp.76.18.04.266]

129. Aman, S.; Naim, A.; Siddiqi, R.; Naz, S. Antimicrobial polyphenols from small tropical fruits, tea and spice oilseeds. Food Sci. Technol. Int.; 2014; 20, pp. 241-251. [DOI: https://dx.doi.org/10.1177/1082013213482476] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/23703103]

130. Premnathan, M.; Chandra, K.; Bajpai, S.K.; Kathiresan, K. A survey of some Indian marine plants for antiviral activity. Bot. Mar.; 1992; 35, pp. 321-324. [DOI: https://dx.doi.org/10.1515/botm.1992.35.4.321]

131. Arunkumar, J.; Rajarajan, S.A. Study on the in vitro Cytotoxicity and Anti-HSV-2 Activity of lyophilized extracts of Terminalia catappa Lin., Mangifera indica Lin. and phytochemical compound mangiferin. Int. J. Med. Pharm. Virol.; 2015; 2, pp. 22-26.

132. Tewtrakul, S.; Miyashiro, H.; Nakamura, N.; Hattori, M.; Kawahata, T.; Otake, T.; Yoshinaga, T.; Fujiwara, T.; Supavita, T.; Yuenyongsawad, S. et al. HIV-1 integrase inhibitory substances from Coleus parvifolius. Phytother. Res.; 2003; 17, pp. 232-239. [DOI: https://dx.doi.org/10.1002/ptr.1111] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/12672152]

133. Hardjito, L. Antibacterial, antioxidant and topoisomerase-I inhibitor activities of the coastal ethnomedicinal plant Pemphis acidula. BIOTROPIA-Southeast Asian J. Trop. Biol.; 2007; 14, pp. 43-51.

134. Samidurai, K.; Saravanakumar, A. Antibacterial activity of Pemphis acidula Forst. Glob. J. Pharmacol.; 2009; 3, pp. 113-115.

135. Abd Wahab, N.Z.; Ja’afar, N.S.A.; Ismail, S.B. Evaluation of antibacterial activity of essential oils of Melaleuca cajuputi Powell. J. Pure Appl. Microbiol.; 2022; 16, pp. 549-557. [DOI: https://dx.doi.org/10.22207/JPAM.16.1.52]

136. Bua, A.; Molicotti, P.; Donadu, M.G.; Usai, D.; Le, L.S.; Tran, T.T.T.; Ngo, V.Q.T.; Marchetti, M.; Usai, M.; Cappuccinelli, P. et al. “In vitro” activity of Melaleuca cajuputi against mycobacterial species. Nat. Prod. Res.; 2020; 34, pp. 1494-1497. [DOI: https://dx.doi.org/10.1080/14786419.2018.1509335]

137. Yala, J.F.; Mabika, R.M.; Camara, B.; Tuo, S.; Souza, A.; Lepengue, A.N.; Koné, D.; M’batchi, B. Assessment of the antibacterial activity of four essential oils and the biobactericide Neco. Int. J. Phytomed; 2017; 9, pp. 443-450. [DOI: https://dx.doi.org/10.5138/09750185.2106]

138. Keereedach, P.; Hrimpeng, K.; Boonbumrung, K. Antifungal activity of Thai cajuput oil and its effect on efflux-pump gene expression in fluconazole-resistant Candida albicans clinical isolates. Int. J. Microbiol.; 2020; 2020, pp. 1-10. [DOI: https://dx.doi.org/10.1155/2020/5989206]

139. Lee, Y.S.; Kim, J.; Shin, S.C.; Lee, S.G.; Park, I.K. Antifungal activity of Myrtaceae essential oils and their components against three phytopathogenic fungi. Flav. Frag. J.; 2008; 23, pp. 23-28. [DOI: https://dx.doi.org/10.1002/ffj.1850]

140. Pino, O.; Sánchez, Y.; Rojas, M.M.; Rodríguez, H.; Abreu, Y.; Duarte, Y.; Martínez, B.; Peteira, B.; Correa, T.M.; Martínez, D. Composición química y actividad plaguicida del aceite esencial de Melaleuca quinquenervia (Cav) ST Blake. Rev. Protección Veg.; 2011; 26, pp. 177-186.

141. Hossain, S.J.; Basar, M.H.; Rokeya, B.; Arif, K.M.T.; Sultana, M.S.; Rahman, M.H. Evaluation of antioxidant, antidiabetic and antibacterial activities of the fruit of Sonneratia apetala (Buch.-Ham.). Oriental Pharm. Exp. Med.; 2013; 13, pp. 95-102. [DOI: https://dx.doi.org/10.1007/s13596-012-0064-4]

142. Afzali, S.F.; Wong, W.L. In vitro screening of Sonneratia alba extract against the oomycete fish pathogen, Aphanomyces invadans. Iran. J. Fish. Sci.; 2017; 16, pp. 1333-1340.

143. Bobbarala, V.; Vadlapudi, V.; Naidu, K.C. Mangrove plant Sonneratia apetala antimicrobial activity on selected pathogenic microorganisms. Orient. J. Chem.; 2009; 25, pp. 445-447.

144. Khumaidah, L.; Purnomo, A.S.; Fatmawati, S. Antimicrobial activity of Sonneratia ovata backer. Hayati J. Biosci.; 2019; 26, 152. [DOI: https://dx.doi.org/10.4308/hjb.26.4.152]

145. Limbago, J.S.; Sosas, J.; Gente, A.A.; Maderse, P.; Rocamora, M.M.; Gomez, D.K. Antibacterial effects of mangrove ethanolic leaf extract against zoonotic fish pathogen Salmonella arizonae. J. Fish.; 2021; 9, 92205. [DOI: https://dx.doi.org/10.17017/j.fish.260]

146. Harizon Pujiastuti, B.; Kurnia, D.; Sumiarsa, D.; Shiono, Y.; Supratman, U. Antibacterial triterpenoids from the bark of Sonneratia alba (Lythraceae). Nat. Prod. Comm.; 2015; 10, pp. 277-280.

147. Gong, K.K.; Li, P.L.; Qiao, D.; Zhang, X.W.; Chu, M.J.; Qin, G.F.; Tang, X.L.; Li, G.Q. Cytotoxic and antiviral triterpenoids from the mangrove plant Sonneratia paracaseolaris. Molecules; 2017; 22, 1319. [DOI: https://dx.doi.org/10.3390/molecules22081319] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/28792469]

148. Moe, T.S.; Win, H.H.; Hlaing, T.T.; Lwin, W.W.; Htet, Z.M.; Mya, K.M. Evaluation of in vitro antioxidant, antiglycation and antimicrobial potential of indigenous Myanmar medicinal plants. J. Integr. Med.; 2018; 16, pp. 358-366. [DOI: https://dx.doi.org/10.1016/j.joim.2018.08.001] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/30120077]

149. Duraipandiyan, V.; Gnanasekar, M.; Ignacimuthu, S. Antifungal activity of triterpenoid isolated from Azima tetracantha leaves. Folia Histochem. Cytobiol; 2010; 48, pp. 311-313. [DOI: https://dx.doi.org/10.2478/v10042-010-0005-3] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/20675291]

150. Sumardi, S.; Basyuni, M.; Wati, R. Antimicrobial activity of polyisoprenoids of sixteen mangrove species from North Sumatra, Indonesia. Biodiversitas J. Biol. Divers; 2018; 19, pp. 1243-1248. [DOI: https://dx.doi.org/10.13057/biodiv/d190409]

151. Abdul-Awal, S.M.; Nazmir, S.; Nasrin, S.; Nurunnabi, T.R.; Uddin, S.J. Evaluation of pharmacological activity of Hibiscus tiliaceus. Springerplus; 2016; 5, pp. 1-6. [DOI: https://dx.doi.org/10.1186/s40064-016-2891-0] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/27516947]

152. Boonsri, S.; Karalai, C.; Ponglimanont, C.; Chantrapromma, S.; Kanjana-Opas, A. Cytotoxic and antibacterial sesquiterpenes from Thespesia populnea. J. Nat. Prod.; 2008; 71, pp. 1173-1177. [DOI: https://dx.doi.org/10.1021/np800055q] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/18553924]

153. Arthanari, S.K.; Vanitha, J.; Ganesh, M.; Venkateshwaran, K.; Clercq, D. Evaluation of antiviral and cytotoxic activities of methanolic extract of S. grandiflora (Fabaceae) flowers. Asian Pac. J. Trop. Biomed.; 2012; 2, pp. S855-S858. [DOI: https://dx.doi.org/10.1016/S2221-1691(12)60323-2]

154. Chungsamarnyart, N.; Sirinarumitr, T.; Chumsing, W.; Wajjawalku, W. In vitro study of antiviral activity of plant crude-extracts against the foot and mouth disease virus. Agric. Nat. Res.; 2007; 41, pp. 97-103.

155. Dey, M.C.; Roy, R.N.; Sinhababu, A. Fatty acid composition and antibacterial activity of the leaf oil of Kleinhovia hospita Linn. J. Nat. Prod.; 2017; 10, pp. 378-384.

156. Rahim, A.; Saito, Y.; Miyake, K.; Goto, M.; Chen, C.H.; Alam, G.; Morris-Natschke, S.; Lee, K.H.; Nakagawa-Goto, K. Kleinhospitine E and cycloartane triterpenoids from Kleinhovia hospita. J. Nat. Prod.; 2018; 81, pp. 1619-1627. [DOI: https://dx.doi.org/10.1021/acs.jnatprod.8b00211] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/30010341]

157. Al Muqarrabun, L.M.R. and Ahmat, N.Medicinal uses, phytochemistry and pharmacology of family Sterculiaceae: A review. Eur. J. Med. Chem.; 2015; 92, pp. 514-530. [DOI: https://dx.doi.org/10.1016/j.ejmech.2015.01.026]

158. Christopher, R.; Nyandoro, S.S.; Chacha, M.; De Koning, C.B. A new cinnamoylglycoflavonoid, antimycobacterial and antioxidant constituents from Heritiera littoralis leaf extracts. Nat. Prod. Res.; 2014; 28, pp. 351-358. [DOI: https://dx.doi.org/10.1080/14786419.2013.863202] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/24443810]

159. Tatsimo, S.J.N.; de Dieu Tamokou, J.; Havyarimana, L.; Csupor, D.; Forgo, P.; Hohmann, J.; Kuiate, J.R.; Tane, P. Antimicrobial and antioxidant activity of kaempferol rhamnoside derivatives from Bryophyllum pinnatum. BMC Res. Notes; 2012; 5, 158. [DOI: https://dx.doi.org/10.1186/1756-0500-5-158] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/22433844]

160. De Almeida, A.P.; Miranda, M.M.F.S.; Simoni, I.C.; Wigg, M.D.; Lagrota, M.H.C.; Costa, S.S. Flavonol monoglycosides isolated from the antiviral fractions of Persea americana (Lauraceae) leaf infusion. Phytother. Res.; 1998; 12, pp. 562-567. [DOI: https://dx.doi.org/10.1002/(SICI)1099-1573(199812)12:8<562::AID-PTR356>3.0.CO;2-6]

161. Kuspradini, H.; Mitsunaga, T.; Ohashi, H. Antimicrobial activity against Streptococcus sobrinus and glucosyltransferase inhibitory activity of taxifolin and some flavanonol rhamnosides from kempas (Koompassia malaccensis) extracts. J. Wood Sci.; 2009; 55, pp. 308-313. [DOI: https://dx.doi.org/10.1007/s10086-009-1026-4]

162. Jiang, R.W.; Ma, S.C.; He, Z.D.; Huang, X.S.; But, P.P.H.; Wang, H.; Chan, S.P.; Ooi, V.E.C.; Xu, H.X.; Mak, T.C. Molecular structurs and antiviral activities of naturally occurring and modified cassane furanoditerpenoids and friedelane triterpenoids from Caesalpinia minax. Bioorg. Med. Chem.; 2002; 10, pp. 2161-2170. [DOI: https://dx.doi.org/10.1016/S0968-0896(02)00072-X]

163. Chang, F.R.; Yen, C.T.; Ei-Shazly, M.; Lin, W.H.; Yen, M.H.; Lin, K.H.; Wu, Y.C. Anti-human coronavirus (anti-HCoV) triterpenoids from the leaves of Euphorbia neriifolia. Nat. Prod. Commun.; 2012; 7, pp. 1415-1417. [DOI: https://dx.doi.org/10.1177/1934578X1200701103]

164. Wangensteen, H.; Dang, H.C.T.; Uddin, S.J.; Alamgir, M.; Malterud, K.E. Antioxidant and antimicrobial effects of the mangrove tree Heritiera fomes. Nat. Prod. Comm.; 2009; 4, pp. 371-376. [DOI: https://dx.doi.org/10.1177/1934578X0900400311]

165. Choudhury, S.; Sree, A.; Mukherjee, S.C.; Pattnaik, P.; Bapuji, M. In vitro antibacterial activity of extracts of selected marine algae and mangroves against fish pathogens. Asian Fish. Sci.; 2005; 18, 285. [DOI: https://dx.doi.org/10.33997/j.afs.2005.18.3.009]

166. Veni, P.S.; Sunita, S.; Srinivasulu, A. Antibacterial and phytochemical screening of Xylocarpus moluccensis leaf and stem on selected drug resistant and sensitive bacteria. Int. J. Microbiol. Res. IJMR; 2014; 5, pp. 30-34.

167. Dai, Y.G.; Wu, J.; Padmakumar, K.P.; Shen, L. Sundarbanxylogranins A–E, five new limonoids from the Sundarban Mangrove, Xylocarpus granatum. Fitoter; 2017; 122, pp. 85-89. [DOI: https://dx.doi.org/10.1016/j.fitote.2017.08.013]

168. Li, W.; Jiang, Z.; Shen, L.; Pedpradab, P.; Bruhn, T.; Wu, J.; Bringmann, G. Antiviral limonoids including khayanolides from the Trang mangrove plant Xylocarpus moluccensis. J. Nat. Prod.; 2015; 78, pp. 1570-1578. [DOI: https://dx.doi.org/10.1021/acs.jnatprod.5b00151]

169. Zhang, Q.; Satyanandamurty, T.; Shen, L.; Wu, J. Krishnolides A–D: New 2-ketokhayanolides from the Krishna mangrove, Xylocarpus moluccensis. Mar. Drugs; 2017; 15, 333. [DOI: https://dx.doi.org/10.3390/md15110333] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/29077062]

170. Pudhom, K.; Sommit, D.; Nuclear, P.; Ngamrojanavanich, N.; Petsom, A. Moluccensins H− J, 30-Ketophragmalin Limonoids from Xylocarpus moluccensis. J. Nat. Prod.; 2010; 73, pp. 263-266. [DOI: https://dx.doi.org/10.1021/np900583h] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/20112995]

171. Du, S.; Wang, M.; Zhu, W.; Qin, Z. A new fungicidal lactone from Xylocarpus granatum (Meliaceae). Nat. Prod. Res.; 2009; 23, pp. 1316-1321. [DOI: https://dx.doi.org/10.1080/14786410902726183] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/19735046]

172. Lesueur, D.; De Rocca Serra, D.; Bighelli, A.; Minh Hoi, T.; Huy Thai, T.; Casanova, J. Composition and antimicrobial activity of the essential oil of Acronychia pedunculata (L.) Miq. from Vietnam. Nat. Prod. Res.; 2008; 22, pp. 393-398. [DOI: https://dx.doi.org/10.1080/14786410701475636] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/18404559]

173. Thirugnanasampandan, R.; Gunasekar, R.; Gogulramnath, M. Chemical composition analysis, antioxidant and antibacterial activity evaluation of essential oil of Atalantia monophylla Correa. Pharmacog. Res.; 2015; 7, S52. [DOI: https://dx.doi.org/10.4103/0974-8490.152009] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/26109788]

174. Trong Le, N.; Viet Ho, D.; Quoc Doan, T.; Tuan Le, A.; Raal, A.; Usai, D.; Sanna, G.; Carta, A.; Rappelli, P.; Diaz, N. et al. Biological activities of essential oils from leaves of Paramignya trimera (Oliv.) Guillaum and Limnocitrus littoralis (Miq.) Swingle. Antibiotics; 2020; 9, 207. [DOI: https://dx.doi.org/10.3390/antibiotics9040207]

175. Reddy, K.H.; Sharma, P.V.G.K.; Reddy, O.V.S. A comparative in vitro study on antifungal and antioxidant activities of Nervilia aragoana and Atlantia monophylla. Pharm. Biol.; 2010; 48, pp. 595-602. [DOI: https://dx.doi.org/10.3109/13880200903218927]

176. Wainwright, M. Acridine—a neglected antibacterial chromophore. J. Antimicrob. Chemother.; 2001; 47, pp. 1-13. [DOI: https://dx.doi.org/10.1093/jac/47.1.1]

177. Thimmaiah, K.; Ugarkar, A.G.; Martis, E.F.; Shaikh, M.S.; Coutinho, E.C.; Yergeri, M.C. Drug–DNA interaction studies of acridone-based derivatives. Nucleosides Nucleotides Nucleic Acids; 2015; 34, pp. 309-331. [DOI: https://dx.doi.org/10.1080/15257770.2014.992531] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/25874941]

178. Manimaran, M.; Rajkumar, T.; Vimal, S.; Taju, G.; Majeed, S.A.; Hameed, A.S.; Kannabiran, K. Antiviral activity of 9 (10H)-Acridanone extracted from marine Streptomyces fradiae strain VITMK2 in Litopenaeus vannamei infected with white spot syndrome virus. Aquaculture; 2018; 488, pp. 66-73. [DOI: https://dx.doi.org/10.1016/j.aquaculture.2018.01.032]

179. Sripisut, T.; Deachathai, S.; Chang, L.C.; Laphookhieo, S. Antibacterial compounds from Atalantia monophylla roots and stems. Planta Med.; 2013; 79, PN11. [DOI: https://dx.doi.org/10.1055/s-0033-1348692]

180. Wisetsai, A.; Lekphrom, R.; Suebrasri, T.; Schevenels, F.T. Acroflavone A, a new prenylated flavone from the fruit of Acronychia pedunculata (L.) Miq. Nat. Prod. Res.; 2021; 36, pp. 5330-5336. [DOI: https://dx.doi.org/10.1080/14786419.2021.1938043] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/34126824]

181. Islam, M.T.; Noor, M.A.; Karon, B.; de Freitas, R.M. In vitro antimicrobial and brine shrimp lethality of Allophylus cobbe L. Ayu; 2012; 33, 299. [DOI: https://dx.doi.org/10.4103/0974-8520.105256]

182. Raghavendra, H.L.; Prashith kekuda T., R.; Karthik K., N.; Ankith G., N. Antiradical, antibacterial, and antifungal activity of Harpullia arborea (Blanco) Radlk. (Sapindaceae). Int. J. Curr. Pharm. Res.; 2017; 9, pp. 32-36.

183. Tumewu, L.; Apryiani, E.; Santi, M.R. Anti Hepatitis C virus activity screening on Harpullia arborea extracts and isolated compound. Proceeding the 1st International Conference on Pharmaceutics and Pharmaceutical Sciences; Fakultas Farmasi Universitas Airlangga: Surabaya, Indonesia, 2014; pp. 165-167.

184. Abdelkader, M.S.A.; Rateb, M.E.; Mohamed, G.A.; Jaspars, M. Harpulliasides A and B: Two new benzeneacetic acid derivatives from Harpullia pendula. Phytochem. Lett.; 2016; 15, pp. 131-135. [DOI: https://dx.doi.org/10.1016/j.phytol.2015.12.006]

185. Anusha, P.; Sudha Bai, R. Phytochemical profile and antimicrobial potential of methanolic extracts of bark and leaf of Quassia indica (Gaertn.) Nooteb. J. Phytopharmacol.; 2017; 6, pp. 269-276. [DOI: https://dx.doi.org/10.31254/phyto.2017.6503]

186. Hardiyanti, R.; Marpaung, L.; Adnyana, I.K.; Simanjuntak, P. Isolation of quercitrin from Dendrophthoe pentandra (L.) Miq leaves and it’s antioxidant and antibacterial activities. Rasayan J. Chem.; 2019; 12, pp. 1822-1827. [DOI: https://dx.doi.org/10.31788/RJC.2019.1235353]

187. Tripathi, S.; Ray, S.; Das, P.K.; Mondal, A.K.; Verma, N.K. Antimicrobial activities of some rare aerial hemi parasitic taxa of south West Bengal, India. Int. J. Phytopharm.; 2013; 4, pp. 106-112.

188. Satish, S.; Raveesha, K.A.; Janardhana, G.R. Antibacterial activity of plant extracts on phytopathogenic Xanthomonas campestris pathovars. Lett. Appl. Microbiol.; 1999; 28, pp. 145-147. [DOI: https://dx.doi.org/10.1046/j.1365-2672.1999.00479.x]

189. Omer, M.E.F.A.; Elnima, E.I. Antimicrobial activity of Ximenia americana. Fitoter; 2003; 74, pp. 122-126. [DOI: https://dx.doi.org/10.1016/S0367-326X(02)00302-7]

190. Owk, A.K.; Lagudu, M.N. Evaluation of antimicrobial activity and phytochemicals in Olax scandens Roxb. roots. Pharma Sci. Monit.; 2016; 7, pp. 232-239.

191. Kone, W.M.; Atindehou, K.K.; Terreaux, C.; Hostettmann, K.; Traore, D.; Dosso, M. Traditional medicine in North Côte-d’Ivoire: Screening of 50 medicinal plants for antibacterial activity. J. Ethnopharmacol.; 2004; 93, pp. 43-49. [DOI: https://dx.doi.org/10.1016/j.jep.2004.03.006]

192. Duraipandiyan, V.; Ayyanar, M.; Ignacimuthu, S. Antimicrobial activity of some ethnomedicinal plants used by Paliyar tribe from Tamil Nadu, India. BMC Compl. Altern. Med.; 2006; 6, pp. 1-7. [DOI: https://dx.doi.org/10.1186/1472-6882-6-35]

193. Asres, K.; Bucar, F.; Kartnig, T.; Witvrouw, M.; Pannecouque, C.; De Clercq, E. Antiviral activity against human immunodeficiency virus type 1 (HIV-1) and type 2 (HIV-2) of ethnobotanically selected Ethiopian medicinal plants. Phytother. Res.; 2001; 15, pp. 62-69. [DOI: https://dx.doi.org/10.1002/1099-1573(200102)15:1<62::AID-PTR956>3.0.CO;2-X]

194. Chandrasekaran, M.; Senthilkumar, A.; Venkatesalu, V. Antibacterial and antifungal efficacy of fatty acid methyl esters from the leaves of Sesuvium portulacastrum L. Eur. Rev. Med. Pharmacol. Sci.; 2011; 15, pp. 775-780.

195. Magwa, M.L.; Gundidza, M.; Gweru, N.; Humphrey, G. Chemical composition and biological activities of essential oil from the leaves of Sesuvium portulacastrum. J. Ethnopharmacol.; 2006; 103, pp. 85-89. [DOI: https://dx.doi.org/10.1016/j.jep.2005.07.024]

196. Bhosale, S.H.; Jagtap, T.G.; Naik, C.G. Antifungal activity of some marine organisms from India, against food spoilage Aspergillus strains. Mycopathologia; 1999; 147, pp. 133-138. [DOI: https://dx.doi.org/10.1023/A:1007184003971]

197. Banerjee, M.B.; Ravikumar, S.; Gnanadesigan, M.; Rajakumar, B.; Anand, M. Antiviral, antioxidant and toxicological evaluation of mangrove associate from South East coast of India. Asian Pac. J. Trop. Biomed.; 2012; 2, pp. S1775-S1779. [DOI: https://dx.doi.org/10.1016/S2221-1691(12)60493-6]

198. Chandrasekaran, M.; Kannathasan, K.; Venkatesalu, V. Antimicrobial activity of fatty acid methyl esters of some members of Chenopodiaceae. Z. Nat. C; 2008; 63, pp. 331-336. [DOI: https://dx.doi.org/10.1515/znc-2008-5-604]

199. Ghosh, D.; Mondal, S.; Ramakrishna, K. Spectroscopic characterization of phytoconstituents isolated from a rare mangrove Aegialitis rotundifolia Roxb., leaves and evaluation of antimicrobial activity of the crude extract. Asian J. Pharm. Clin. Res.; 2019; 12, pp. 220-224. [DOI: https://dx.doi.org/10.22159/ajpcr.2019.v12i9.29986]

200. Sett, S.; Hazra, J.; Datta, S.; Mitra, A.; Mitra, A.K. Screening the Indian Sundarban mangrove for antimicrobial activity. Int. J. Sci. Innov. Disc.; 2014; 4, pp. 17-25.

201. Min, B.S.; Kim, Y.H.; Tomiyama, M.; Nakamura, N.; Miyashiro, H.; Otake, T.; Hattori, M. Inhibitory effects of Korean plants on HIV-1 activities. Phytother. Res.; 2001; 15, pp. 481-486. [DOI: https://dx.doi.org/10.1002/ptr.751] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/11536375]

202. Sahoo, S.; Panda, P.K.; Mishra, S.R.; Parida, R.K.; Ellaiah, P.; Dash, S.K. Antibacterial activity of Barringtonia acutangula against selected urinary tract pathogens. Indian J. Pharma Sci.; 2008; 70, 677. [DOI: https://dx.doi.org/10.4103/0250-474X.45417] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/21394275]

203. Mishra, S.; Sahoo, S.; Mishra, S.K.; Rout, K.K.; Nayak, S.K.; Panda, P.K.; Dhal, N.K. Antimicrobial investigation of leaves of Barringtonia acutangula Linn. Med. Aromat. Plant Sci. Biotechnol.; 2009; 3, pp. 55-58.

204. Khan, M.R.; Omoloso, A.D. Antibacterial, antifungal activities of Barringtonia asiatica. Fitoter; 2002; 73, pp. 255-260. [DOI: https://dx.doi.org/10.1016/S0367-326X(02)00067-9]

205. Hussin, N.M.; Muse, R.; Ahmad, S.; Ramli, J.; Mahmood, M.; Sulaiman, M.R.; Shukor, M.Y.A.; Rahman, M.F.A.; Aziz, K.N.K. Antifungal activity of extracts and phenolic compounds from Barringtonia racemosa L.(Lecythidaceae). African J. Biotechnol.; 2009; 8, pp. 2835-2842.

206. Saha, S.; Sarkar, K.K.; Hossain, M.L.; Hossin, A.; Barman, A.K.; Ahmed, M.I.; Sadhu, S.K. Bioactivity studies on Barringtonia racemosa (Lam.) bark. Pharmacologyonline; 2013; 1, pp. 93-100.

207. Ragasa, C.Y.; Espineli, D.L.; Shen, C.C. New triterpenes from Barringtonia asiatica. Chem. Pharm. Bull.; 2011; 59, pp. 778-782. [DOI: https://dx.doi.org/10.1248/cpb.59.778] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/21628919]

208. Bonvicini, F.; Antognoni, F.; Mandrone, M.; Protti, M.; Mercolini, L.; Lianza, M.; Gentilomi, G.A.; Poli, F. Phytochemical analysis and antibacterial activity towards methicillin-resistant Staphylococcus aureus of leaf extracts from Argania spinosa (L.) Skeels. Plant Biosystem.; 2017; 151, pp. 649-656. [DOI: https://dx.doi.org/10.1080/11263504.2016.1190418]

209. Rahman, M.M.; Polfreman, D.; MacGeachan, J.; Gray, A.I. Antimicrobial activities of Barringtonia acutangula. Phytother. Res.; 2005; 19, pp. 543-545. [DOI: https://dx.doi.org/10.1002/ptr.1341] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/16114086]

210. Pefile, S.C. A Study of the Antiherpes Simplex Virus Type 1 Properties of Barringtonia racemosa. Ph.D. Thesis; University of Cape: Cape Town, Africa, 2001.

211. Janmanchi, H.; Raju, A.; Degani, M.S.; Ray, M.K.; Rajan, M.G.R. Antituberculosis, antibacterial and antioxidant activities of Aegiceras corniculatum, a mangrove plant and effect of various extraction processes on its phytoconstituents and bioactivity. S. Afr. J. Bot.; 2017; 113, pp. 421-427. [DOI: https://dx.doi.org/10.1016/j.sajb.2017.09.019]

212. Gupta, V.K.; Mukherjee, K.; Roy, A. Two novel antifungals, acornine 1 and acornine 2, from the bark of mangrove plant Aegiceras corniculatum (Linn.) Blanco from Sundarban Estuary. Pharmacog. Mag.; 2014; 10, S342.

213. Nariya, P.B.; Bhalodia, N.R.; Shukla, V.J.; Acharya, R.N. Antimicrobial and antifungal activities of Cordia dichotoma (Forster F.) bark extracts. Ayu; 2011; 32, 585. [DOI: https://dx.doi.org/10.4103/0974-8520.96138] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/22661859]

214. Li, S.; Zhang, Z.; Cain, A.; Wang, B.; Long, M.; Taylor, J. Antifungal activity of camptothecin, trifolin, and hyperoside isolated from Camptotheca acuminata. J. Agric. Food Chem.; 2005; 53, pp. 32-37. [DOI: https://dx.doi.org/10.1021/jf0484780]

215. Horwitz, S.B.; Chang, C.K.; Grollman, A.P. Antiviral action of camptothecin. Antimicrob. Agents Chemother.; 1972; 2, pp. 395-401. [DOI: https://dx.doi.org/10.1128/AAC.2.5.395] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/4363789]

216. Wu, K.X.; Chu, J.J.H. Antiviral screen identifies EV71 inhibitors and reveals camptothecin-target, DNA topoisomerase 1 as a novel EV71 host factor. Antiv. Res.; 2017; 143, pp. 122-133. [DOI: https://dx.doi.org/10.1016/j.antiviral.2017.04.008] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/28427827]

217. Kelly, D.C.; Avery, R.J.; Dimmock, N.J. Camptothecin: An inhibitor of influenza virus replication. J. Gen. Virol.; 1974; 25, pp. 427-432. [DOI: https://dx.doi.org/10.1099/0022-1317-25-3-427] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/4475096]

218. Rubinstein, L.; Rein, A. Effect of camptothecin on Simian virus 40 DNA. Nature; 1974; 248, pp. 226-228. [DOI: https://dx.doi.org/10.1038/248226a0]

219. Pantazis, P. Camptothecin: A promising antiretroviral drug. J. Biomed. Sci.; 1996; 3, pp. 14-19. [DOI: https://dx.doi.org/10.1007/BF02253574] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/11725078]

220. Ali, A.M.; Mackeen, M.M.; El-Sharkawy, S.H.; Hamid, J.A.; Ismail, N.H.; Ahmad, F.; Lajis, N.H. Antiviral and cytotoxic activities of some plants used in Malaysian indigenous medicine. Pertanika J. Trop. Agric. Sci.; 1996; 19, pp. 129-136.

221. Ahmed, F.; Amin, R.; Shahid, I.Z.; Sobhani, M.M.E. Antibacterial, cytotoxic and neuropharmacological activities of Cerbera odollam seeds. Adv. Trad. Med.; 2008; 8, pp. 323-328. [DOI: https://dx.doi.org/10.3742/OPEM.2008.8.4.323]

222. Chu, S.Y.; Singh, H.; Ahmad, M.S.; Mamat, A.S. Phytochemical screening of antifungal biocompounds from fruits and leaves extract of Cerbera odollam Gaertn. Malays. Appl. Biol.; 2015; 44, pp. 75-79.

223. Pájaro-González, Y.; Cabrera-Barraza, J.; Martelo-Ramírez, G.; Oliveros-Díaz, A.F.; Urrego-Álvarez, J.; Quiñones-Fletcher, W.; Díaz-Castillo, F. In Vitro and In Silico Antistaphylococcal Activity of Indole Alkaloids Isolated from Tabernaemontana cymosa Jacq (Apocynaceae). Sci. Pharm.; 2022; 90, 38. [DOI: https://dx.doi.org/10.3390/scipharm90020038]

224. Ahmed, F.; Reza, M.S.H.; Shahid, I.Z.; Khatun, A.; Islam, K.K.; Ali, M.R. Antibacterial and antinociceptive activity of Hoya parasitica. Hamdard Med.; 2008; 51, pp. 22-26.

225. Muangrom, W.; Vajrodaya, S. Comparative phytochemistry and antibacterial properties of Guettarda speciosa L. Proceedings of the 56th Kasetsart University Annual Conference; Bangkok, Thailand, 30 January–2 February 2018.

226. Prachayasittikul, S.; Buraparuangsang, P.; Worachartcheewan, A.; Isarankura-Na-Ayudhya, C.; Ruchirawat, S.; Prachayasittikul, V. Antimicrobial and antioxidative activities of bioactive constituents from Hydnophytum formicarum Jack. Molecules; 2008; 13, pp. 904-921. [DOI: https://dx.doi.org/10.3390/molecules13040904] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/18463592]

227. Bachala, T. Antibacterial and Antifungal activities of various extracts of Guettarda speciosa L. Int. J. Phytopharmacol.; 2010; 1, pp. 20-22.

228. Zhang, H.; Rothwangl, K.; Mesecar, A.D.; Sabahi, A.; Rong, L.; Fong, H.H. Lamiridosins, hepatitis C virus entry inhibitors from Lamium album. J. Nat. Prod.; 2009; 72, pp. 2158-2162. [DOI: https://dx.doi.org/10.1021/np900549e]

229. Ge, L.; Wan, H.; Tang, S.; Chen, H.; Li, J.; Zhang, K.; Zhou, B.; Fei, J.; Wu, S.; Zeng, X. Novel caffeoylquinic acid derivatives from Lonicera japonica Thunb. flower buds exert pronounced anti-HBV activities. RSC Adv.; 2018; 8, pp. 35374-35385. [DOI: https://dx.doi.org/10.1039/C8RA07549B] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/35547940]

230. De Carvalho Junior, A.R.; Oliveira Ferreira, R.; de Souza Passos, M.; da Silva Boeno, S.I.; Glória das Virgens, L.D.L.; Ventura, T.L.B.; Calixto, S.D.; Lassounskaia, E.; de Carvalho, M.G.; Braz-Filho, R. et al. Antimycobacterial and nitric oxide production inhibitory activities of triterpenes and alkaloids from Psychotria nuda (Cham. & Schltdl.) Wawra. Molecules; 2019; 24, 1026.

231. Hanh, N.P.; Phan, N.H.T.; Thuan, N.T.D.; Hanh, T.T.H.; Vien, L.T.; Thao, N.P.; Thanh, N.V.; Cuong, N.X.; Binh, N.Q.; Nam, N.H. et al. Two new simple iridoids from the ant-plant Myrmecodia tuberosa and their antimicrobial effects. Nat. Prod. Res.; 2016; 30, pp. 2071-2076. [DOI: https://dx.doi.org/10.1080/14786419.2015.1113412]

232. Kapadia, G.J.; Sharma, S.C.; Tokuda, H.; Nishino, H.; Ueda, S. Inhibitory effect of iridoids on Epstein-Barr virus activation by a short-term in vitro assay for anti-tumor promoters. Cancer Lett.; 1996; 102, pp. 223-226. [DOI: https://dx.doi.org/10.1016/0304-3835(96)04184-5]

233. Pollo, L.A.; Martin, E.F.; Machado, V.R.; Cantillon, D.; Wildner, L.M.; Bazzo, M.L.; Waddell, S.J.; Biavatti, M.W.; Sandjo, L.P. Search for antimicrobial activity among fifty-two natural and synthetic compounds identifies anthraquinone and polyacetylene classes that inhibit Mycobacterium tuberculosis. Front. Microbiol.; 2021; 11, 622629. [DOI: https://dx.doi.org/10.3389/fmicb.2020.622629] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/33537021]

234. Manzione, M.G.; Martorell, M.; Sharopov, F.; Bhat, N.G.; Kumar, N.V.A.; Fokou, P.V.T.; Pezzani, R. Phytochemical and pharmacological properties of asperuloside, a systematic review. Eur. J. Pharmacol.; 2020; 883, 173344. [DOI: https://dx.doi.org/10.1016/j.ejphar.2020.173344]

235. Mahmood, N.; Moore, P.S.; De Tommasi, N.; De Simone, F.; Colman, S.; Hay, A.J.; Pizza, C. Inhibition of HIV infection by caffeoylquinic acid derivatives. Antiv. Chem. Chemother.; 1993; 4, pp. 235-240. [DOI: https://dx.doi.org/10.1177/095632029300400406]

236. Ticona, L.A.; Bermejo, P.; Guerra, J.A.; Abad, M.J.; Beltran, M.; Lázaro, R.M.; Alcamí, J.; Bedoya, L.M. Ethanolic extract of Artemisia campestris subsp. glutinosa (Besser) Batt. inhibits HIV–1 replication in vitro through the activity of terpenes and flavonoids on viral entry and NF–κB pathway. J. Ethnopharmacol.; 2020; 263, 113163. [DOI: https://dx.doi.org/10.1016/j.jep.2020.113163]

237. Chokchaisiri, R.; Suaisom, C.; Sriphota, S.; Chindaduang, A.; Chuprajob, T.; Suksamrarn, A. Bioactive flavonoids of the flowers of Butea monosperma. Chem. Pharm. Bull.; 2009; 57, pp. 428-432. [DOI: https://dx.doi.org/10.1248/cpb.57.428]

238. Kuo, Y.C.; Chen, C.C.; Tsai, W.J.; Ho, Y.H. Regulation of herpes simplex virus type 1 replication in Vero cells by Psychotria serpens: Relationship to gene expression, DNA replication, and protein synthesis. Antiv. Res.; 2001; 51, pp. 95-109. [DOI: https://dx.doi.org/10.1016/S0166-3542(01)00141-3]

239. Yu, S.; Liu, B.C.; Lai, P.X. Chemical composition, antibacterial and antioxidant activities of the essential oil of Psychotria serpens. Chem. Nat. Comp.; 2020; 56, pp. 748-750. [DOI: https://dx.doi.org/10.1007/s10600-020-03138-4]

240. Bose, S.; Bose, A. Antimicrobial activity of Acanthus ilicifolius (L.). Indian J. Pharm. Sci.; 2008; 70, 821. [DOI: https://dx.doi.org/10.4103/0250-474X.49134] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/21369453]

241. Ravikumar, S.; Raja, M.; Gnanadesigan, M. Antibacterial potential of benzoate and phenylethanoid derivatives isolated from Acanthus ilicifolius L. leaf extracts. Nat. Prod. Res.; 2012; 26, pp. 2270-2273. [DOI: https://dx.doi.org/10.1080/14786419.2011.652962] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/22292885]

242. Wei, P.H.; Wu, S.Z.; Mu, X.M.; Xu, B.; Su, Q.J.; Wei, J.L.; Yang, Y.; Qin, B.; Xie, Z.C. Effect of alcohol extract of Acanthus ilicifolius L. on anti-duck hepatitis B virus and protection of liver. J. Ethnopharmacol.; 2015; 160, pp. 1-5. [DOI: https://dx.doi.org/10.1016/j.jep.2014.10.050] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/25446633]

243. Illian, D.N.; Basyuni, M.; Wati, R.; Hasibuan, P.A.Z. Polyisoprenoids from Avicennia marina and Avicennia lanata inhibit WiDr cells proliferation. Pharmacog. Mag.; 2018; 14, 513.

244. Lalitha, P.; Parthiban, A.; Sachithanandam, V.; Purvaja, R.; Ramesh, R. Antibacterial and antioxidant potential of GC-MS analysis of crude ethyl acetate extract from the tropical mangrove plant Avicennia officinalis L. S. Afr. J. Bot.; 2021; 142, pp. 149-155. [DOI: https://dx.doi.org/10.1016/j.sajb.2021.06.023]

245. Vadlapudi, V.; Naidu, K.C. Bioactivity of marine mangrove plant Avicennia alba on selected plant and oral pathogens. Int. J. ChemTech Res.; 2009; 1, pp. 1213-1216.

246. Subrahmanyam, C.; Kumar, S.R.; Reddy, G.D. Bioactive diterpenes from the mangrove Avicennia officinalis Linn. Indian J. Chem.; 2006; 45, pp. 2556-2557. [DOI: https://dx.doi.org/10.1002/chin.200711156]

247. Nguyen, T.S.; Xia, N.H.; Van Chu, T.; Van Sam, H. Ethnobotanical study on medicinal plants in traditional markets of Son La province, Vietnam. For. Soc.; 2019; 3, pp. 171-192. [DOI: https://dx.doi.org/10.24259/fs.v3i2.6005]

248. Chen, J.L.; Blanc, P.; Stoddart, C.A.; Bogan, M.; Rozhon, E.J.; Parkinson, N.; Ye, Z.; Cooper, R.; Balick, M.; Nanakorn, W. et al. New iridoids from the medicinal plant Barleria prionitis with potent activity against respiratory syncytial virus. J. Nat. Prod.; 1998; 61, pp. 1295-1297. [DOI: https://dx.doi.org/10.1021/np980086y]

249. Yecheng, D.; Zhen, Y.; Yanzhen, Y.; Xiulian, B. Inhibitory activity against plant pathogenic fungi of extracts from Myoporum bontioides A. Gray and indentification of active ingredients. Pest Manag. Sci.; 2008; 64, pp. 203-207. [DOI: https://dx.doi.org/10.1002/ps.1491]

250. Dong, L.M.; Huang, L.L.; Dai, H.; Xu, Q.L.; Ouyang, J.K.; Jia, X.C.; Gu, W.X.; Tan, J.W. Anti-MRSA sesquiterpenes from the semi-mangrove plant Myoporum bontioides A. Gray. Mar. Drugs; 2018; 16, 438. [DOI: https://dx.doi.org/10.3390/md16110438] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/30413080]

251. Minh, T.T.; Toan, H.K.; Quang, L.D.; Hoang, V.D. Myobontioids AD and antifungal metabolites from the leaves of Myoporum bontioides A. Gray. Nat. Prod. Res.; 2021; pp. 1-7. [DOI: https://dx.doi.org/10.1080/14786419.2021.2016747] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/34927497]

252. Lirio, S.B.; Macabeo, A.P.G.; Paragas, E.M.; Knorn, M.; Kohls, P.; Franzblau, S.G.; Wang, Y.; Aguinaldo, M.A.M. Antitubercular constituents from Premna odorata Blanco. J. Ethnopharmacol.; 2014; 154, pp. 471-474. [DOI: https://dx.doi.org/10.1016/j.jep.2014.04.015] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/24768632]

253. Tangarife-Castaño, V.; Roa-Linares, V.; Betancur-Galvis, L.A.; Durán García, D.C.; Stashenko, E.; Mesa-Arango, A.C. Antifungal activity of Verbenaceae and Labiatae families essential oils. Pharmacologyonline; 2012; 1, pp. 133-145.

254. Rahman, A.; Shanta, Z.S.; Rashid, M.A.; Parvin, T.; Afrin, S.; Khatun, M.K.; Sattar, M.A. In vitro antibacterial properties of essential oil and organic extracts of Premna integrifolia Linn. Arabian J. Chem.; 2016; 9, pp. S475-S479. [DOI: https://dx.doi.org/10.1016/j.arabjc.2011.06.003]

255. Nguyen, Q.V.; Eun, J.B. Antimicrobial activity of some Vietnamese medicinal plants extracts. J. Med. Plants Res.; 2013; 4, pp. 2597-2605.

256. Sheeba, S.N.; Ariharan, V.N.; Mary, J.V.J.; Bai, S.M.M.; Paul, J.V. Phytochemical and biological screening of organic Solvent extracts of Ipomoea pes-caprae flower. Ann. Rom. Soc. Cell Biol.; 2021; 25, pp. 7800-7821.

257. Ryan, D.H.; Katherine, H.H.; Taylor, J.W.; Gajendra, S. Traditional Tongan treatments for infections: Bioassays and ethnobotanical leads for activity. J. Med. Plants Res.; 2014; 8, pp. 1215-1222.

258. Srimoon, R.; Ngiewthaisong, S. Antioxidant and antibacterial activities of Indian marsh fleabane (Pluchea indica (L.) Less). Asia-Pac. J. Sci. Technol.; 2015; 20, pp. 144-154.

259. Locher, C.P.; Witvrouw, M.; De Béthune, M.P.; Burch, M.T.; Mower, H.F.; Davis, H.; Lasure, A.; Pauwels, R.; De Clercq, E.; Vlietinck, A.J. Antiviral activity of Hawaiian medicinal plants against human immunodeficiency virus type-1 (HIV-1). Phytomed; 1996; 2, pp. 259-264. [DOI: https://dx.doi.org/10.1016/S0944-7113(96)80052-3]

260. Manimegalai, B.; Inbathamizh, L.; Ponnu, T.M. In vitro studies on antimicrobial activity and phytochemical screening of leaf extracts of Scaevola taccada. Int. J. Pharm. Pharm. Sci.; 2012; 4, pp. 367-370.

261. Suthiwong, J.; Thongsri, Y.; Yenjai, C. A new furanocoumarin from the fruits of Scaevola taccada and antifungal activity against Pythium insidiosum. Nat. Prod. Res.; 2017; 31, pp. 453-459. [DOI: https://dx.doi.org/10.1080/14786419.2016.1188100] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/27223164]

262. Rameshthangam, P.A.; Ramasamy, P. Antiviral activity of bis (2-methylheptyl) phthalate isolated from Pongamia pinnata leaves against White Spot Syndrome Virus of Penaeus monodon Fabricius. Virus Res.; 2007; 126, pp. 38-44. [DOI: https://dx.doi.org/10.1016/j.virusres.2007.01.014] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/17328984]

263. Sudheer, N.S.; Philip, R.; Singh, I.B. In vivo screening of mangrove plants for anti WSSV activity in Penaeus monodon, and evaluation of Ceriops tagal as a potential source of antiviral molecules. Aquacult; 2011; 311, pp. 36-41. [DOI: https://dx.doi.org/10.1016/j.aquaculture.2010.11.016]

264. Rahmawati, N.; Mustofa, F.I.; Haryanti, S. Diversity of medicinal plants utilized by To Manui ethnic of Central Sulawesi, Indonesia. Biodiversitas J. Biol. Divers.; 2020; 21, pp. 375-392. [DOI: https://dx.doi.org/10.13057/biodiv/d210145]

265. Chusri, S.; Sinvaraphan, N.; Chaipak, P.; Luxsananuwong, A.; Voravuthikunchai, S.P. Evaluation of antibacterial activity, phytochemical constituents, and cytotoxicity effects of Thai household ancient remedies. J. Altern. Compl. Med.; 2014; 20, pp. 909-918. [DOI: https://dx.doi.org/10.1089/acm.2013.0173]

266. Swamy, V.; Ninge, K.; Sudhakar, R. Antimicrobial activity of Casuarina equisetifolia. Int. J. Innov. Pharm. Dev.; 2013; 1, pp. 49-57.

267. Buenz, E.J. Hepatocytes detoxify Atuna racemosa extract. Exp. Biol. Med.; 2006; 231, pp. 1739-1743. [DOI: https://dx.doi.org/10.1177/153537020623101111]

268. Wiart, C. Medicinal Plants in the Asia Pacific for Zoonotic Pandemics; CRC Press: Boca Raton, FL, USA, 2021.

269. Brijesh, S.; Daswani, P.G.; Tetali, P.; Rojatkar, S.R.; Antia, N.H.; Birdi, T.J. Studies on Pongamia pinnata (L.) Pierre leaves: Understanding the mechanism(s) of action in infectious diarrhea. J. Zhejiang Univ. Sci. B.; 2006; 7, pp. 665-674. [DOI: https://dx.doi.org/10.1631/jzus.2006.B0665]

270. Thaman, R.R.; Thomson, L.A.; DeMeo, R.; Areki, F.; Elevitch, C.R. Intsia bijuga (vesi). Species Profiles for Pacific Island Agroforestry; Academic Publishing: Cambridge, MA, USA, 2006.

271. Islam, A.R.; Hasan, M.M.; Islam, M.T.; Tanaka, N. Ethnobotanical study of plants used by the Munda ethnic group living around the Sundarbans, the world’s largest mangrove forest in southwestern Bangladesh. J. Ethnopharmacol.; 2022; 285, 114853. [DOI: https://dx.doi.org/10.1016/j.jep.2021.114853]

272. Walker, T. An Examination of Medicinal Ethnobotany and Biomedicine Use in Two Villages on the Phnom Kulen Plateau; Hollins University: Roanoke, VA, USA, 2017.

273. Li, D.L.; Xing, F.W. Ethnobotanical study on medicinal plants used by local Hoklos people on Hainan Island, China. J. Ethnopharmacol.; 2016; 194, pp. 358-368. [DOI: https://dx.doi.org/10.1016/j.jep.2016.07.050] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/27444693]

274. Duraipandiyan, V.; Ignacimuthu, S. Antifungal activity of traditional medicinal plants from Tamil Nadu, India. Asian Pac. J. Trop. Biomed; 2011; 1, pp. S204-S215. [DOI: https://dx.doi.org/10.1016/S2221-1691(11)60157-3]

275. Ju, S.K.; Semotiuk, A.J.; Krishna, V. Indigenous knowledge on medicinal plants used by ethnic communities of South India. Ethnobot. Res. Appl.; 2019; 18, pp. 1-112.

276. Janni, K. Plants in Samoan Culture. The Ethnobotany of Samoa. Econ. Bot.; 2002; 56, 100. [DOI: https://dx.doi.org/10.1663/0013-0001(2002)056[0100:PISCTE]2.0.CO;2]

277. Herlina, R.; Rahayuningsih, M.; Iswari, R.S. Species richness of medicinal plants in the Dieng Plateau. J. Innov. Sci. Educ.; 2019; 8, pp. 116-122.

278. Uy, M.M.; Garcia, K.I. Evaluation of the antioxidant properties of the leaf extracts of Philippine medicinal plants Casuarina equisetifolia Linn, Cyperus brevifolius (Rottb) Hassk, Drymoglossum piloselloides Linn, Ixora chinensis Lam, and Piper abbreviatum Opiz. Adv. Agric. Bot.; 2015; 7, pp. 71-79.

279. Tomar, S.; Jawanjal, P. Overview of Pentatropis capensis (Asclepiadaceae)—An extra pharmacopoeial plant. J. Ayu Herb. Med.; 2019; 5, pp. 66-69. [DOI: https://dx.doi.org/10.31254/jahm.2019.5207]

280. Wiart, C. Medicinal Plants of Asia and the Pacific; Drugs for the Future?; World Scientific Publishing Co. Inc.: Singapore, 2006.

281. Thomson, L.A.; Englberger, L.; Guarino, L.; Thaman, R.R.; Elevitch, C.R. Pandanus tectorius (pandanus). Species Profiles for Pacific Island Agroforestry; ResearchGate GmbH: Berlin, Germany, 2006; 28.

282. Medhi, R.P.; Chakrabarti, S. Traditional knowledge of NE people on conservation of wild orchids. Indian J. Tradit. Knowl.; 2009; 8, pp. 11-16.

283. Akhter, M.; Hoque, M.M.; Rahman, M.; Huda, M.K. Ethnobotanical investigation of some orchids used by five communities of Cox’s Bazar and Chittagong hill tracts districts of Bangladesh. J. Med. Plants Stud.; 2017; 5, pp. 265-268.

284. Rahmatullah, M.; Mollik, M.A.H.; Islam, M.K.; Islam, M.R.; Jahan, F.I.; Khatun, Z.; Seraj, S.; Chowdhury, M.H.; Islam, F.; Miajee, Z.U.M. et al. A survey of medicinal and functional food plants used by the folk medicinal practitioners of three villages in Sreepur Upazilla, Magura district, Bangladesh. Am. Eurasian J. Sustain. Agric.; 2010; 4, pp. 363-373.

285. Primavera, J.; Sadaba, R.; Lebata, M.; Hazel, J.; Altamirano, J. Handbook of Mangroves in the Philippines-Panay; Aquaculture Department, Southeast Asian Fisheries Development Center: Tigbauan, Philippines, 2004.

286. Latayada, F.S.; Uy, M.M. Screening of the antioxidant properties of the leaf extracts of Philippine medicinal plants Ficus nota (Blanco) Merr., Metroxylon sagu Rottb., Mussaenda philippica A. Rich., Inocarpus fagifer, and Cinnamomum mercadoi Vidal. Bull. Environ. Pharmacol. Life Sci.; 2016; 5, pp. 18-24.

287. Wiart, C. Ethnopharmacology of Medicinal Plants: Asia and the Pacific; Springer Science & Business Media: Berlin/Heidelberg, Germany, 2007.

288. Motley, T.J. The ethnobotany of Fagraea Thunb. (Gentianaceae): The timber of malesia and the scent of polynesia. Econ. Bot.; 2004; 58, pp. 396-409. [DOI: https://dx.doi.org/10.1663/0013-0001(2004)058[0396:TEOFTG]2.0.CO;2]

289. Paramita, S. Tahongai (Kleinhovia hospita L.): Review sebuah tumbuhan obat dari Kalimantan Timur. Indones. J. Plant Med.; 2016; 9, pp. 29-36. [DOI: https://dx.doi.org/10.22435/toi.v9i1.6390.29-36]

290. Duke, N.C. Australia’s Mangroves: The Authoritative Guide to Australia’s Mangrove Plants; MER: Brisbane, Australia, 2006.

291. Liebezeit, G.; Rau, M.T. New Guinean mangroves—Traditional usage and chemistry of natural products. Senckenberg. Marit.; 2006; 36, pp. 1-10. [DOI: https://dx.doi.org/10.1007/BF03043698]

292. Cambie, R.C.; Ash, J. Fijian Medicinal Plants; CSIRO Publishing: Clayton, Australia, 1994.

293. Khare, C.P. Indian Medicinal Plants: An Illustrated Dictionary; Springer Science & Business Media: Berlin/Heidelberg, Germany, 2008.

294. Reverter, M.; Bontemps, N.N.; Lecchini, D.; Banaigs, B.; Sasal, P. Use of plant extracts in fish aquaculture as an alternative to chemotherapy: Current status and future perspectives. Aquaculture; 2014; 433, pp. 50-61. [DOI: https://dx.doi.org/10.1016/j.aquaculture.2014.05.048]

295. Soto-Rodriguez, S.A.; Gomez-Gil, B.; Lozano, R.; del Rio-Rodríguez, R.l.; Diéguez, A.L.; Romalde, J.L. Virulence of Vibrio harveyi responsible for the “Bright-red” Syndrome in the Pacific white shrimp Litopenaeus vannamei. J. Invertebr. Pathol.; 2012; 109, pp. 307-317. [DOI: https://dx.doi.org/10.1016/j.jip.2012.01.006]

296. Davies, T.K.; Lovelock, C.E.; Pettit, N.E.; Grierson, P.F. Short-term microbial respiration in an arid zone mangrove soil is limited by availability of gallic acid, phosphorus and ammonium. Soil Biol. Biochem.; 2017; 115, pp. 73-81. [DOI: https://dx.doi.org/10.1016/j.soilbio.2017.08.010]

297. Liu, Y.; Li, F.; Huang, Q. Allelopathic effects of gallic acid from Aegiceras corniculatum on Cyclotella caspia. J. Env. Sci.; 2013; 25, pp. 776-784. [DOI: https://dx.doi.org/10.1016/S1001-0742(12)60112-0]

298. Alonso-Rodrıguez, R.; Páez-Osuna, F. Nutrients, phytoplankton and harmful algal blooms in shrimp ponds: A review with special reference to the situation in the Gulf of California. Aquaculture; 2003; 219, pp. 317-336. [DOI: https://dx.doi.org/10.1016/S0044-8486(02)00509-4]

299. Gao, J.; Zuo, H.; Yang, L.; He, J.H.; Niu, S.; Weng, S.; He, J.; Xu, X. Long-term influence of cyanobacterial bloom on the immune system of Litopenaeus vannamei. Fish Shellfish. Immunol.; 2017; 61, pp. 79-85. [DOI: https://dx.doi.org/10.1016/j.fsi.2016.12.015] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/27986602]

300. Gil-Turnes, M.S.; Hay, M.E.; Fenical, W. Symbiotic marine bacteria chemically defend crustacean embryos from a pathogenic fungus. Science; 1989; 246, pp. 116-118. [DOI: https://dx.doi.org/10.1126/science.2781297]

301. Haoliang, L.; Chongling, Y.; Jingchun, L. Low-molecular-weight organic acids exuded by Mangrove (Kandelia candel (L.) Druce) roots and their effect on cadmium species change in the rhizosphere. Environ. Exp. Bot.; 2007; 61, pp. 159-166. [DOI: https://dx.doi.org/10.1016/j.envexpbot.2007.05.007]

302. White, S.L.; Rainbow, P.S. Regulation and accumulation of copper, zinc and cadmium by the shrimp Palaemon elegans. Mar. Ecol. Prog. Ser.; 1982; 8, pp. 95-101. [DOI: https://dx.doi.org/10.3354/meps008095]

303. Rozirwan, R.; Muda, H.I.; Ulqodry, T.Z. Antibacterial potential of Actinomycetes isolated from mangrove sediment in Tanjung Api-Api, South Sumatra, Indonesia. Biodiversitas J. Biol. Divers; 2020; 21, pp. 5723-5728. [DOI: https://dx.doi.org/10.13057/biodiv/d211232]